Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP289731.RAvv9A6o3dyovr8hWtHrF7AG6F11QqLOFbNjnMjaBJf4c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP289731.RAvv9A6o3dyovr8hWtHrF7AG6F11QqLOFbNjnMjaBJf4c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP289731.RAvv9A6o3dyovr8hWtHrF7AG6F11QqLOFbNjnMjaBJf4c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP289731.RAvv9A6o3dyovr8hWtHrF7AG6F11QqLOFbNjnMjaBJf4c130_provenance.
- NP289731.RAvv9A6o3dyovr8hWtHrF7AG6F11QqLOFbNjnMjaBJf4c130_assertion description "[Of these, only two (one BCC and one AK) harboured simultaneously mutations of p16, but with no consequence on p16beta transcript.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP289731.RAvv9A6o3dyovr8hWtHrF7AG6F11QqLOFbNjnMjaBJf4c130_provenance.
- NP289731.RAvv9A6o3dyovr8hWtHrF7AG6F11QqLOFbNjnMjaBJf4c130_assertion evidence source_evidence_literature NP289731.RAvv9A6o3dyovr8hWtHrF7AG6F11QqLOFbNjnMjaBJf4c130_provenance.
- NP289731.RAvv9A6o3dyovr8hWtHrF7AG6F11QqLOFbNjnMjaBJf4c130_assertion SIO_000772 10498902 NP289731.RAvv9A6o3dyovr8hWtHrF7AG6F11QqLOFbNjnMjaBJf4c130_provenance.
- NP289731.RAvv9A6o3dyovr8hWtHrF7AG6F11QqLOFbNjnMjaBJf4c130_assertion wasDerivedFrom befree-20140225 NP289731.RAvv9A6o3dyovr8hWtHrF7AG6F11QqLOFbNjnMjaBJf4c130_provenance.
- NP289731.RAvv9A6o3dyovr8hWtHrF7AG6F11QqLOFbNjnMjaBJf4c130_assertion wasGeneratedBy ECO_0000203 NP289731.RAvv9A6o3dyovr8hWtHrF7AG6F11QqLOFbNjnMjaBJf4c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP289731.RAvv9A6o3dyovr8hWtHrF7AG6F11QqLOFbNjnMjaBJf4c130_provenance.