Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP446500.RA-8a1Mpd2-Q2BihvEygjFe6iaVJ9Aum9fLDBxBE7dZJw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP446500.RA-8a1Mpd2-Q2BihvEygjFe6iaVJ9Aum9fLDBxBE7dZJw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446500.RA-8a1Mpd2-Q2BihvEygjFe6iaVJ9Aum9fLDBxBE7dZJw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446500.RA-8a1Mpd2-Q2BihvEygjFe6iaVJ9Aum9fLDBxBE7dZJw130_provenance.
- NP446500.RA-8a1Mpd2-Q2BihvEygjFe6iaVJ9Aum9fLDBxBE7dZJw130_assertion description "[This study emphasizes that modifiers such as CD46 and FHL-1 may determine the kidney phenotype of patients who present with homozygous CFH deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446500.RA-8a1Mpd2-Q2BihvEygjFe6iaVJ9Aum9fLDBxBE7dZJw130_provenance.
- NP446500.RA-8a1Mpd2-Q2BihvEygjFe6iaVJ9Aum9fLDBxBE7dZJw130_assertion evidence source_evidence_literature NP446500.RA-8a1Mpd2-Q2BihvEygjFe6iaVJ9Aum9fLDBxBE7dZJw130_provenance.
- NP446500.RA-8a1Mpd2-Q2BihvEygjFe6iaVJ9Aum9fLDBxBE7dZJw130_assertion SIO_000772 23870792 NP446500.RA-8a1Mpd2-Q2BihvEygjFe6iaVJ9Aum9fLDBxBE7dZJw130_provenance.
- NP446500.RA-8a1Mpd2-Q2BihvEygjFe6iaVJ9Aum9fLDBxBE7dZJw130_assertion wasDerivedFrom befree-20150227 NP446500.RA-8a1Mpd2-Q2BihvEygjFe6iaVJ9Aum9fLDBxBE7dZJw130_provenance.
- NP446500.RA-8a1Mpd2-Q2BihvEygjFe6iaVJ9Aum9fLDBxBE7dZJw130_assertion wasGeneratedBy ECO_0000203 NP446500.RA-8a1Mpd2-Q2BihvEygjFe6iaVJ9Aum9fLDBxBE7dZJw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP446500.RA-8a1Mpd2-Q2BihvEygjFe6iaVJ9Aum9fLDBxBE7dZJw130_provenance.