Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP887717.RAz03xqN5XoQolfdWLvtjlMwmLsMR6yEnsYZQMExiVIp0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP887717.RAz03xqN5XoQolfdWLvtjlMwmLsMR6yEnsYZQMExiVIp0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887717.RAz03xqN5XoQolfdWLvtjlMwmLsMR6yEnsYZQMExiVIp0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887717.RAz03xqN5XoQolfdWLvtjlMwmLsMR6yEnsYZQMExiVIp0130_provenance.
- NP887717.RAz03xqN5XoQolfdWLvtjlMwmLsMR6yEnsYZQMExiVIp0130_assertion description "[In addition, we identify the Factor H-like protein 1 (FHL-1), an alternative splice product of the CFH gene as an additional protein that includes the risk residue 402, and thus confers risk for AMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887717.RAz03xqN5XoQolfdWLvtjlMwmLsMR6yEnsYZQMExiVIp0130_provenance.
- NP887717.RAz03xqN5XoQolfdWLvtjlMwmLsMR6yEnsYZQMExiVIp0130_assertion evidence source_evidence_literature NP887717.RAz03xqN5XoQolfdWLvtjlMwmLsMR6yEnsYZQMExiVIp0130_provenance.
- NP887717.RAz03xqN5XoQolfdWLvtjlMwmLsMR6yEnsYZQMExiVIp0130_assertion SIO_000772 17399790 NP887717.RAz03xqN5XoQolfdWLvtjlMwmLsMR6yEnsYZQMExiVIp0130_provenance.
- NP887717.RAz03xqN5XoQolfdWLvtjlMwmLsMR6yEnsYZQMExiVIp0130_assertion wasDerivedFrom befree-20150227 NP887717.RAz03xqN5XoQolfdWLvtjlMwmLsMR6yEnsYZQMExiVIp0130_provenance.
- NP887717.RAz03xqN5XoQolfdWLvtjlMwmLsMR6yEnsYZQMExiVIp0130_assertion wasGeneratedBy ECO_0000203 NP887717.RAz03xqN5XoQolfdWLvtjlMwmLsMR6yEnsYZQMExiVIp0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP887717.RAz03xqN5XoQolfdWLvtjlMwmLsMR6yEnsYZQMExiVIp0130_provenance.