Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1399108.RANqA_0S5Rj9Q10807ThQKGIAqJCTkJV0b5Q_zZqaFtCc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1399108.RANqA_0S5Rj9Q10807ThQKGIAqJCTkJV0b5Q_zZqaFtCc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1399108.RANqA_0S5Rj9Q10807ThQKGIAqJCTkJV0b5Q_zZqaFtCc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1399108.RANqA_0S5Rj9Q10807ThQKGIAqJCTkJV0b5Q_zZqaFtCc130_provenance.
- NP1399108.RANqA_0S5Rj9Q10807ThQKGIAqJCTkJV0b5Q_zZqaFtCc130_assertion description "[There was a higher frequency of APOE epsilon4 alleles in patients with AD (30%, P=0.016) and VD (26%, P=0.07) compared with control subjects (15%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1399108.RANqA_0S5Rj9Q10807ThQKGIAqJCTkJV0b5Q_zZqaFtCc130_provenance.
- NP1399108.RANqA_0S5Rj9Q10807ThQKGIAqJCTkJV0b5Q_zZqaFtCc130_assertion evidence source_evidence_literature NP1399108.RANqA_0S5Rj9Q10807ThQKGIAqJCTkJV0b5Q_zZqaFtCc130_provenance.
- NP1399108.RANqA_0S5Rj9Q10807ThQKGIAqJCTkJV0b5Q_zZqaFtCc130_assertion SIO_000772 9660395 NP1399108.RANqA_0S5Rj9Q10807ThQKGIAqJCTkJV0b5Q_zZqaFtCc130_provenance.
- NP1399108.RANqA_0S5Rj9Q10807ThQKGIAqJCTkJV0b5Q_zZqaFtCc130_assertion wasDerivedFrom befree-2016 NP1399108.RANqA_0S5Rj9Q10807ThQKGIAqJCTkJV0b5Q_zZqaFtCc130_provenance.
- NP1399108.RANqA_0S5Rj9Q10807ThQKGIAqJCTkJV0b5Q_zZqaFtCc130_assertion wasGeneratedBy ECO_0000203 NP1399108.RANqA_0S5Rj9Q10807ThQKGIAqJCTkJV0b5Q_zZqaFtCc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1399108.RANqA_0S5Rj9Q10807ThQKGIAqJCTkJV0b5Q_zZqaFtCc130_provenance.