List of serched triples
A total of 22252 records found
#21792
high Confidence
Subject:
SCNEC
(Tumor)
→
is
→
Object:
rare_highly_aggressive_tumor
(Tumor phenotype)
Original: Small cell neuroendocrine carcinoma (SCNEC)#is#a rare/ highly aggressive tumor with poor prognosis
#21791
high Confidence
Subject:
masses
(Tumor tissue)
→
identified_as
→
Object:
meningotheliomatous_meningiomas
(Tumor type)
Original: masses#identified as#meningotheliomatous meningiomas with atypical features
#21790
high Confidence
Subject:
tumor
(Tumor tissue)
→
reveals
→
Object:
SMARCA4_deep_deletion
(Gene deletion)
Original: tumor#revealed#SMARCA4 deep deletion
#21789
high Confidence
Subject:
Systemic_anaplastic_large_cell_lymphoma
(Tumor)
→
was_treated_with
→
Object:
CHOP
(Chemotherapy drugs)
Original: patient#was put on#a regime of CHOP and is disease-free 33 months after diagnosis
#21788
high Confidence
Subject:
tumor_cells
(Tumor cells)
→
expressed
→
Object:
ALK1
(protein)
Original: tumor cells#expressed#CD30/ CD45/ EMA/ and ALK-1
#21787
high Confidence
Subject:
tumor_cells
(Tumor cells)
→
expressed
→
Object:
EMA
(protein)
Original: tumor cells#expressed#CD30/ CD45/ EMA/ and ALK-1
#21786
high Confidence
Subject:
tumor_cells
(Tumor cells)
→
expressed
→
Object:
CD45
(protein)
Original: tumor cells#expressed#CD30/ CD45/ EMA/ and ALK-1
#21785
high Confidence
Subject:
tumor_cells
(Tumor cells)
→
expressed
→
Object:
CD30
(protein)
Original: tumor cells#expressed#CD30/ CD45/ EMA/ and ALK-1
#21784
high Confidence
Subject:
Gastric-type endocervical adenocarcinoma (GAS)
(Tumor subtype)
→
is_variant_of
→
Object:
cervical_adenocarcinoma
(Tumor type)
Original: GAS#is#a clinically aggressive variant of cervical adenocarcinoma
#21783
high Confidence
Subject:
GLUT2
(Glucose transporter)
→
mutations_cause
→
Object:
Fanconi-Bickel_syndrome
(Single gene disease)
Original: Fanconi-Bickel syndrome#is caused by#mutations in the GLUT2 (SLC2A2) gene
#21782
high Confidence
Subject:
S100
(protein)
→
is_upregulated_in
→
Object:
melanoma
(Tumor)
Original: melanoma#is characterized by#large pleomorphic cells with eosinophilic cytoplasm/ prominent nucleoli/ and S100 protein
#21781
high Confidence
Subject:
CCND1_copy_number_gain
(Genomic changes)
→
is_associated_with
→
Object:
poor_prognosis
(Disease phenotype)
Original: increased copy number gains in 11q (cyclin D1)#is associated with#poor prognosis in melanoma
#21780
high Confidence
Subject:
Extraskeletal_myxoid_chondrosarcoma
(Neoplastic diseases)
→
is_characterized_by
→
Object:
recurrent_chromosomal_translocation_involving_NR4A3
(Genomic abnormalities)
Original: Extraskeletal myxoid chondrosarcoma (EMC)#is characterized by#recurrent chromosomal translocation involving NR4A3
#21779
high Confidence
Subject:
lymphocytic_smear_background
(Cell morphology)
→
indicates
→
Object:
type_B_thymomas
(Tumor type)
Original: lymphocytic smear background#indicated#type B thymomas in 87.5% of cases
#21778
high Confidence
Subject:
NUT_midline_carcinoma
(Tumor diseases)
→
shows_positive_immunostaining_with
→
Object:
NUT_antibody
(Diagnostic Antibodies)
Original: NMC#has#characteristic morphological features and positive immunostaining with NUT antibody
#21777
high Confidence
Subject:
NUT
(Protein coding genes)
→
rearrangement_detected_by
→
Object:
RT-PCR
(Diagnostic techniques)
Original: The diagnosis of NMC#is made by#demonstration of NUT rearrangement via immunohistochemistry/ FISH/ or RT-PCR
#21776
high Confidence
Subject:
NUT
(Protein coding genes)
→
rearrangement_detected_by
→
Object:
FISH
(Diagnostic techniques)
Original: The diagnosis of NMC#is made by#demonstration of NUT rearrangement via immunohistochemistry/ FISH/ or RT-PCR
#21775
high Confidence
Subject:
NUT
(Protein coding genes)
→
rearrangement_detected_by
→
Object:
Immunohistochemistry
(Diagnostic techniques)
Original: The diagnosis of NMC#is made by#demonstration of NUT rearrangement via immunohistochemistry/ FISH/ or RT-PCR
#21774
high Confidence
Subject:
NUT
(Protein coding genes)
→
chromosomal_rearrangement_of
→
Object:
NUT_at_15q14
(Chromosome structural variation)
Original: NMC#is characterized by#chromosomal rearrangements of the gene NUT at 15q14
#21773
high Confidence
Subject:
Fluorescence_in_situ_hybridisation_technique
(Molecular detection technology)
→
has_established_its_role_in
→
Object:
diagnosis_of_lymphoid_malignancies
(Tumor disease diagnosis)
Original: Fluorescence in-situ hybridisation technique#has established its role in#diagnosis of lymphoid malignancies