Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_provenance.
- NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_assertion description "[Levels of lipoprotein(a) are primarily determined by variation in the LPA gene coding for the apolipoprotein(a) moiety of lipoprotein(a), and genetic epidemiologic studies have documented association of LPA copy number variants, influencing levels of lipoprotein(a), with risk of IHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_provenance.
- NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_assertion evidence source_evidence_literature NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_provenance.
- NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_assertion SIO_000772 20106478 NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_provenance.
- NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_assertion wasDerivedFrom befree-20140225 NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_provenance.
- NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_assertion wasGeneratedBy ECO_0000203 NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_provenance.