Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP240838.RAmka9BGZaU7lYiFnjkV6a3rWdo3FHfkxGFMdEHSZFOkI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP240838.RAmka9BGZaU7lYiFnjkV6a3rWdo3FHfkxGFMdEHSZFOkI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP240838.RAmka9BGZaU7lYiFnjkV6a3rWdo3FHfkxGFMdEHSZFOkI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP240838.RAmka9BGZaU7lYiFnjkV6a3rWdo3FHfkxGFMdEHSZFOkI130_provenance.
- NP240838.RAmka9BGZaU7lYiFnjkV6a3rWdo3FHfkxGFMdEHSZFOkI130_assertion description "[Several apoE and LPL gene variants affecting CAD risk, plasma TG or apoB concentrations have an allelic frequency of >5% in the general population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP240838.RAmka9BGZaU7lYiFnjkV6a3rWdo3FHfkxGFMdEHSZFOkI130_provenance.
- NP240838.RAmka9BGZaU7lYiFnjkV6a3rWdo3FHfkxGFMdEHSZFOkI130_assertion evidence source_evidence_literature NP240838.RAmka9BGZaU7lYiFnjkV6a3rWdo3FHfkxGFMdEHSZFOkI130_provenance.
- NP240838.RAmka9BGZaU7lYiFnjkV6a3rWdo3FHfkxGFMdEHSZFOkI130_assertion SIO_000772 17848837 NP240838.RAmka9BGZaU7lYiFnjkV6a3rWdo3FHfkxGFMdEHSZFOkI130_provenance.
- NP240838.RAmka9BGZaU7lYiFnjkV6a3rWdo3FHfkxGFMdEHSZFOkI130_assertion wasDerivedFrom befree-20140225 NP240838.RAmka9BGZaU7lYiFnjkV6a3rWdo3FHfkxGFMdEHSZFOkI130_provenance.
- NP240838.RAmka9BGZaU7lYiFnjkV6a3rWdo3FHfkxGFMdEHSZFOkI130_assertion wasGeneratedBy ECO_0000203 NP240838.RAmka9BGZaU7lYiFnjkV6a3rWdo3FHfkxGFMdEHSZFOkI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP240838.RAmka9BGZaU7lYiFnjkV6a3rWdo3FHfkxGFMdEHSZFOkI130_provenance.