Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP278871.RAgCxeeAjAV_7i_iwH3TSUqCkpgKLrPRAaLLsFoPJ1i4U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP278871.RAgCxeeAjAV_7i_iwH3TSUqCkpgKLrPRAaLLsFoPJ1i4U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP278871.RAgCxeeAjAV_7i_iwH3TSUqCkpgKLrPRAaLLsFoPJ1i4U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP278871.RAgCxeeAjAV_7i_iwH3TSUqCkpgKLrPRAaLLsFoPJ1i4U130_provenance.
- NP278871.RAgCxeeAjAV_7i_iwH3TSUqCkpgKLrPRAaLLsFoPJ1i4U130_assertion description "[In familial cutaneous malignant melanoma (CMM), disruption of the retinoblastoma (pRB) pathway frequently occurs through inactivating mutations in the p16 (p16INK4A/CDKN2A/MTS1) gene or activating mutations in the G1-specific cyclin dependent kinase 4 gene (CDK4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP278871.RAgCxeeAjAV_7i_iwH3TSUqCkpgKLrPRAaLLsFoPJ1i4U130_provenance.
- NP278871.RAgCxeeAjAV_7i_iwH3TSUqCkpgKLrPRAaLLsFoPJ1i4U130_assertion evidence source_evidence_literature NP278871.RAgCxeeAjAV_7i_iwH3TSUqCkpgKLrPRAaLLsFoPJ1i4U130_provenance.
- NP278871.RAgCxeeAjAV_7i_iwH3TSUqCkpgKLrPRAaLLsFoPJ1i4U130_assertion SIO_000772 10732752 NP278871.RAgCxeeAjAV_7i_iwH3TSUqCkpgKLrPRAaLLsFoPJ1i4U130_provenance.
- NP278871.RAgCxeeAjAV_7i_iwH3TSUqCkpgKLrPRAaLLsFoPJ1i4U130_assertion wasDerivedFrom befree-2016 NP278871.RAgCxeeAjAV_7i_iwH3TSUqCkpgKLrPRAaLLsFoPJ1i4U130_provenance.
- NP278871.RAgCxeeAjAV_7i_iwH3TSUqCkpgKLrPRAaLLsFoPJ1i4U130_assertion wasGeneratedBy ECO_0000203 NP278871.RAgCxeeAjAV_7i_iwH3TSUqCkpgKLrPRAaLLsFoPJ1i4U130_provenance.
- befree-2016 importedOn "2016-02-19" NP278871.RAgCxeeAjAV_7i_iwH3TSUqCkpgKLrPRAaLLsFoPJ1i4U130_provenance.