Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP338169.RAeaBDCruh6Azfhna4caDB5jvyy5P916hHWOFSXirEg5o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP338169.RAeaBDCruh6Azfhna4caDB5jvyy5P916hHWOFSXirEg5o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP338169.RAeaBDCruh6Azfhna4caDB5jvyy5P916hHWOFSXirEg5o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP338169.RAeaBDCruh6Azfhna4caDB5jvyy5P916hHWOFSXirEg5o130_provenance.
- NP338169.RAeaBDCruh6Azfhna4caDB5jvyy5P916hHWOFSXirEg5o130_assertion description "[No associations were found with the AR (GGC)(n), CYP17 Msp A1 I, VDR Taq I, SRD5A2 (TA)(n) and p.49A >T polymorphisms and CaP risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338169.RAeaBDCruh6Azfhna4caDB5jvyy5P916hHWOFSXirEg5o130_provenance.
- NP338169.RAeaBDCruh6Azfhna4caDB5jvyy5P916hHWOFSXirEg5o130_assertion evidence source_evidence_literature NP338169.RAeaBDCruh6Azfhna4caDB5jvyy5P916hHWOFSXirEg5o130_provenance.
- NP338169.RAeaBDCruh6Azfhna4caDB5jvyy5P916hHWOFSXirEg5o130_assertion SIO_000772 15711606 NP338169.RAeaBDCruh6Azfhna4caDB5jvyy5P916hHWOFSXirEg5o130_provenance.
- NP338169.RAeaBDCruh6Azfhna4caDB5jvyy5P916hHWOFSXirEg5o130_assertion wasDerivedFrom befree-20140225 NP338169.RAeaBDCruh6Azfhna4caDB5jvyy5P916hHWOFSXirEg5o130_provenance.
- NP338169.RAeaBDCruh6Azfhna4caDB5jvyy5P916hHWOFSXirEg5o130_assertion wasGeneratedBy ECO_0000203 NP338169.RAeaBDCruh6Azfhna4caDB5jvyy5P916hHWOFSXirEg5o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP338169.RAeaBDCruh6Azfhna4caDB5jvyy5P916hHWOFSXirEg5o130_provenance.