Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP610168.RA7erD0aXEVjfyt-RcKIVmwNa3GQDbGgfQADO3S_QWpf0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP610168.RA7erD0aXEVjfyt-RcKIVmwNa3GQDbGgfQADO3S_QWpf0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP610168.RA7erD0aXEVjfyt-RcKIVmwNa3GQDbGgfQADO3S_QWpf0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP610168.RA7erD0aXEVjfyt-RcKIVmwNa3GQDbGgfQADO3S_QWpf0130_provenance.
- NP610168.RA7erD0aXEVjfyt-RcKIVmwNa3GQDbGgfQADO3S_QWpf0130_assertion description "[Germline mutations of the CDKN2A and CDK4 genes explain a significant proportion of familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610168.RA7erD0aXEVjfyt-RcKIVmwNa3GQDbGgfQADO3S_QWpf0130_provenance.
- NP610168.RA7erD0aXEVjfyt-RcKIVmwNa3GQDbGgfQADO3S_QWpf0130_assertion evidence source_evidence_literature NP610168.RA7erD0aXEVjfyt-RcKIVmwNa3GQDbGgfQADO3S_QWpf0130_provenance.
- NP610168.RA7erD0aXEVjfyt-RcKIVmwNa3GQDbGgfQADO3S_QWpf0130_assertion SIO_000772 17505264 NP610168.RA7erD0aXEVjfyt-RcKIVmwNa3GQDbGgfQADO3S_QWpf0130_provenance.
- NP610168.RA7erD0aXEVjfyt-RcKIVmwNa3GQDbGgfQADO3S_QWpf0130_assertion wasDerivedFrom befree-2016 NP610168.RA7erD0aXEVjfyt-RcKIVmwNa3GQDbGgfQADO3S_QWpf0130_provenance.
- NP610168.RA7erD0aXEVjfyt-RcKIVmwNa3GQDbGgfQADO3S_QWpf0130_assertion wasGeneratedBy ECO_0000203 NP610168.RA7erD0aXEVjfyt-RcKIVmwNa3GQDbGgfQADO3S_QWpf0130_provenance.
- befree-2016 importedOn "2016-02-19" NP610168.RA7erD0aXEVjfyt-RcKIVmwNa3GQDbGgfQADO3S_QWpf0130_provenance.