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- source_evidence_literature type ECO_0000212 NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_provenance.
- NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_assertion description "[Occurrence of structural genetic alterations was analyzed in 18 seminomas and 22 non-seminomas for genes involved in the malignant tumour phenotype: cadherin 1, Type 1, E-cadherin (Epithelial), CDH1; adenomatous polyposis coli, APC; NME/NM23 nucleoside diphosphate kinase 1, NME1; tumour protein P53, TP53; cyclin-dependent kinase inhibitor 2A, CDKN2A; retinoblastoma 1, RB1; RAD51 recombinase, RAD51; mutS homolog 2, MSH2; MutL homolog 1, MLH1; breast cancer 1, early onset, BRCA1; BCL2-Associated X Protein, BAX; ATP-Binding Cassette, Sub-Family G (WHITE), Member 2, ABCG2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_provenance.
- NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_assertion evidence source_evidence_literature NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_provenance.
- NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_assertion SIO_000772 25075023 NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_provenance.
- NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_assertion wasDerivedFrom befree-20150227 NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_provenance.
- NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_assertion wasGeneratedBy ECO_0000203 NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_provenance.