Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP259231.RAyjgB6j7sRmBqQoiHafASKFsOtEccqbnLekd_CtT5z6I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP259231.RAyjgB6j7sRmBqQoiHafASKFsOtEccqbnLekd_CtT5z6I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP259231.RAyjgB6j7sRmBqQoiHafASKFsOtEccqbnLekd_CtT5z6I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP259231.RAyjgB6j7sRmBqQoiHafASKFsOtEccqbnLekd_CtT5z6I130_provenance.
- NP259231.RAyjgB6j7sRmBqQoiHafASKFsOtEccqbnLekd_CtT5z6I130_assertion description "[Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259231.RAyjgB6j7sRmBqQoiHafASKFsOtEccqbnLekd_CtT5z6I130_provenance.
- NP259231.RAyjgB6j7sRmBqQoiHafASKFsOtEccqbnLekd_CtT5z6I130_assertion evidence source_evidence_literature NP259231.RAyjgB6j7sRmBqQoiHafASKFsOtEccqbnLekd_CtT5z6I130_provenance.
- NP259231.RAyjgB6j7sRmBqQoiHafASKFsOtEccqbnLekd_CtT5z6I130_assertion SIO_000772 10431236 NP259231.RAyjgB6j7sRmBqQoiHafASKFsOtEccqbnLekd_CtT5z6I130_provenance.
- NP259231.RAyjgB6j7sRmBqQoiHafASKFsOtEccqbnLekd_CtT5z6I130_assertion wasDerivedFrom befree-2016 NP259231.RAyjgB6j7sRmBqQoiHafASKFsOtEccqbnLekd_CtT5z6I130_provenance.
- NP259231.RAyjgB6j7sRmBqQoiHafASKFsOtEccqbnLekd_CtT5z6I130_assertion wasGeneratedBy ECO_0000203 NP259231.RAyjgB6j7sRmBqQoiHafASKFsOtEccqbnLekd_CtT5z6I130_provenance.
- befree-2016 importedOn "2016-02-19" NP259231.RAyjgB6j7sRmBqQoiHafASKFsOtEccqbnLekd_CtT5z6I130_provenance.