Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_provenance.
- NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_assertion description "[Similar to its existing use in the diagnosis of monogenic dyslipidemias such as familial hypercholesterolemia, clinical inquiry regarding family history was identified as an important determinant of eligibility for APOE genotyping performed in the context of chronic disease risk management.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_provenance.
- NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_assertion evidence source_evidence_literature NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_provenance.
- NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_assertion SIO_000772 25731628 NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_provenance.
- NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_assertion wasDerivedFrom befree-2016 NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_provenance.
- NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_assertion wasGeneratedBy ECO_0000203 NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_provenance.