Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1346834.RAYtpb97UpCPifO1p17sxmBYKCSuwGqEAqygFd4GXG-vE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1346834.RAYtpb97UpCPifO1p17sxmBYKCSuwGqEAqygFd4GXG-vE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1346834.RAYtpb97UpCPifO1p17sxmBYKCSuwGqEAqygFd4GXG-vE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1346834.RAYtpb97UpCPifO1p17sxmBYKCSuwGqEAqygFd4GXG-vE130_provenance.
- NP1346834.RAYtpb97UpCPifO1p17sxmBYKCSuwGqEAqygFd4GXG-vE130_assertion description "[A common FGFR3 gene mutation in hypochondroplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1346834.RAYtpb97UpCPifO1p17sxmBYKCSuwGqEAqygFd4GXG-vE130_provenance.
- NP1346834.RAYtpb97UpCPifO1p17sxmBYKCSuwGqEAqygFd4GXG-vE130_assertion evidence source_evidence_literature NP1346834.RAYtpb97UpCPifO1p17sxmBYKCSuwGqEAqygFd4GXG-vE130_provenance.
- NP1346834.RAYtpb97UpCPifO1p17sxmBYKCSuwGqEAqygFd4GXG-vE130_assertion SIO_000772 8589686 NP1346834.RAYtpb97UpCPifO1p17sxmBYKCSuwGqEAqygFd4GXG-vE130_provenance.
- NP1346834.RAYtpb97UpCPifO1p17sxmBYKCSuwGqEAqygFd4GXG-vE130_assertion wasDerivedFrom befree-2016 NP1346834.RAYtpb97UpCPifO1p17sxmBYKCSuwGqEAqygFd4GXG-vE130_provenance.
- NP1346834.RAYtpb97UpCPifO1p17sxmBYKCSuwGqEAqygFd4GXG-vE130_assertion wasGeneratedBy ECO_0000203 NP1346834.RAYtpb97UpCPifO1p17sxmBYKCSuwGqEAqygFd4GXG-vE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1346834.RAYtpb97UpCPifO1p17sxmBYKCSuwGqEAqygFd4GXG-vE130_provenance.