Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP49878.RA1vL_TpSiyAI4LaQcmOSx6LOwhd5NJkFcMJ4f6Z9QdPk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP49878.RA1vL_TpSiyAI4LaQcmOSx6LOwhd5NJkFcMJ4f6Z9QdPk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP49878.RA1vL_TpSiyAI4LaQcmOSx6LOwhd5NJkFcMJ4f6Z9QdPk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP49878.RA1vL_TpSiyAI4LaQcmOSx6LOwhd5NJkFcMJ4f6Z9QdPk130_provenance.
- NP49878.RA1vL_TpSiyAI4LaQcmOSx6LOwhd5NJkFcMJ4f6Z9QdPk130_assertion description "[A cohort of 1002 heterozygous FH patients was genotyped for polymorphisms in the genes encoding for ATP-binding cassette transporter A1, apolipoprotein (apo) AIV, apoCIII, apoE, cholesteryl transfer ester protein, hepatic lipase, lipoprotein lipase, and two paraoxonases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49878.RA1vL_TpSiyAI4LaQcmOSx6LOwhd5NJkFcMJ4f6Z9QdPk130_provenance.
- NP49878.RA1vL_TpSiyAI4LaQcmOSx6LOwhd5NJkFcMJ4f6Z9QdPk130_assertion evidence source_evidence_literature NP49878.RA1vL_TpSiyAI4LaQcmOSx6LOwhd5NJkFcMJ4f6Z9QdPk130_provenance.
- NP49878.RA1vL_TpSiyAI4LaQcmOSx6LOwhd5NJkFcMJ4f6Z9QdPk130_assertion SIO_000772 16030523 NP49878.RA1vL_TpSiyAI4LaQcmOSx6LOwhd5NJkFcMJ4f6Z9QdPk130_provenance.
- NP49878.RA1vL_TpSiyAI4LaQcmOSx6LOwhd5NJkFcMJ4f6Z9QdPk130_assertion wasDerivedFrom gad-20130706 NP49878.RA1vL_TpSiyAI4LaQcmOSx6LOwhd5NJkFcMJ4f6Z9QdPk130_provenance.
- NP49878.RA1vL_TpSiyAI4LaQcmOSx6LOwhd5NJkFcMJ4f6Z9QdPk130_assertion wasGeneratedBy ECO_0000203 NP49878.RA1vL_TpSiyAI4LaQcmOSx6LOwhd5NJkFcMJ4f6Z9QdPk130_provenance.
- gad-20130706 importedOn "2013-07-06" NP49878.RA1vL_TpSiyAI4LaQcmOSx6LOwhd5NJkFcMJ4f6Z9QdPk130_provenance.