Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_provenance.
- NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_assertion description "[Our results support the following conclusions: (i) somatic mutation of the CDKN2 gene is rare in sporadic melanomas with allelic loss at 9p21; (ii) homozygous loss is more frequent than mutation of the CDKN2 gene in sporadic melanomas; (iii) at 9p21-p23 genes other than CDKN2 may be involved in the development of sporadic melanomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_provenance.
- NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_assertion evidence source_evidence_literature NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_provenance.
- NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_assertion SIO_000772 8631588 NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_provenance.
- NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_assertion wasDerivedFrom befree-20140225 NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_provenance.
- NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_assertion wasGeneratedBy ECO_0000203 NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_provenance.