Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP134107.RAXPQ0z_V-C6xlkbRZn69PS8KtILRSYgYxd4f2y7o8IWo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP134107.RAXPQ0z_V-C6xlkbRZn69PS8KtILRSYgYxd4f2y7o8IWo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP134107.RAXPQ0z_V-C6xlkbRZn69PS8KtILRSYgYxd4f2y7o8IWo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP134107.RAXPQ0z_V-C6xlkbRZn69PS8KtILRSYgYxd4f2y7o8IWo130_provenance.
- NP134107.RAXPQ0z_V-C6xlkbRZn69PS8KtILRSYgYxd4f2y7o8IWo130_assertion description "[The mutant 128R allele of the E-selectin gene is associated with angiographic severe coronary artery disease (CAD) in Saudi Arabs/association is lost after adjustment for traditional CAD risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP134107.RAXPQ0z_V-C6xlkbRZn69PS8KtILRSYgYxd4f2y7o8IWo130_provenance.
- NP134107.RAXPQ0z_V-C6xlkbRZn69PS8KtILRSYgYxd4f2y7o8IWo130_assertion evidence source_evidence_literature NP134107.RAXPQ0z_V-C6xlkbRZn69PS8KtILRSYgYxd4f2y7o8IWo130_provenance.
- NP134107.RAXPQ0z_V-C6xlkbRZn69PS8KtILRSYgYxd4f2y7o8IWo130_assertion SIO_000772 16756647 NP134107.RAXPQ0z_V-C6xlkbRZn69PS8KtILRSYgYxd4f2y7o8IWo130_provenance.
- NP134107.RAXPQ0z_V-C6xlkbRZn69PS8KtILRSYgYxd4f2y7o8IWo130_assertion wasDerivedFrom lhgdn-20090331 NP134107.RAXPQ0z_V-C6xlkbRZn69PS8KtILRSYgYxd4f2y7o8IWo130_provenance.
- NP134107.RAXPQ0z_V-C6xlkbRZn69PS8KtILRSYgYxd4f2y7o8IWo130_assertion wasGeneratedBy ECO_0000203 NP134107.RAXPQ0z_V-C6xlkbRZn69PS8KtILRSYgYxd4f2y7o8IWo130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP134107.RAXPQ0z_V-C6xlkbRZn69PS8KtILRSYgYxd4f2y7o8IWo130_provenance.