Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP83577.RA2P-U1uHQWgCtHE2Apax5VSNMjh4FmItCZwEUDHQXmFI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP83577.RA2P-U1uHQWgCtHE2Apax5VSNMjh4FmItCZwEUDHQXmFI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP83577.RA2P-U1uHQWgCtHE2Apax5VSNMjh4FmItCZwEUDHQXmFI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP83577.RA2P-U1uHQWgCtHE2Apax5VSNMjh4FmItCZwEUDHQXmFI130_provenance.
- NP83577.RA2P-U1uHQWgCtHE2Apax5VSNMjh4FmItCZwEUDHQXmFI130_assertion description "[genetic variants in the FAS and FASLG genes may contribute to the etiology of CMM in the general population, particularly in those with a low risk of sunlight-induced CMM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83577.RA2P-U1uHQWgCtHE2Apax5VSNMjh4FmItCZwEUDHQXmFI130_provenance.
- NP83577.RA2P-U1uHQWgCtHE2Apax5VSNMjh4FmItCZwEUDHQXmFI130_assertion evidence source_evidence_literature NP83577.RA2P-U1uHQWgCtHE2Apax5VSNMjh4FmItCZwEUDHQXmFI130_provenance.
- NP83577.RA2P-U1uHQWgCtHE2Apax5VSNMjh4FmItCZwEUDHQXmFI130_assertion SIO_000772 16538172 NP83577.RA2P-U1uHQWgCtHE2Apax5VSNMjh4FmItCZwEUDHQXmFI130_provenance.
- NP83577.RA2P-U1uHQWgCtHE2Apax5VSNMjh4FmItCZwEUDHQXmFI130_assertion wasDerivedFrom gad-20150221 NP83577.RA2P-U1uHQWgCtHE2Apax5VSNMjh4FmItCZwEUDHQXmFI130_provenance.
- NP83577.RA2P-U1uHQWgCtHE2Apax5VSNMjh4FmItCZwEUDHQXmFI130_assertion wasGeneratedBy ECO_0000203 NP83577.RA2P-U1uHQWgCtHE2Apax5VSNMjh4FmItCZwEUDHQXmFI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP83577.RA2P-U1uHQWgCtHE2Apax5VSNMjh4FmItCZwEUDHQXmFI130_provenance.