Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP887369.RABcikVSVUirR10WxW7ARBkY3373p7skFupYL1vSjKvck130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP887369.RABcikVSVUirR10WxW7ARBkY3373p7skFupYL1vSjKvck130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887369.RABcikVSVUirR10WxW7ARBkY3373p7skFupYL1vSjKvck130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887369.RABcikVSVUirR10WxW7ARBkY3373p7skFupYL1vSjKvck130_provenance.
- NP887369.RABcikVSVUirR10WxW7ARBkY3373p7skFupYL1vSjKvck130_assertion description "[In summary, the PSMD9 IVS3+nt460A/G, +nt437C/T and exon E197G A/G SNPs are linked to CAD, stroke/TIA and macrovascular pathology of T2D in Italians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887369.RABcikVSVUirR10WxW7ARBkY3373p7skFupYL1vSjKvck130_provenance.
- NP887369.RABcikVSVUirR10WxW7ARBkY3373p7skFupYL1vSjKvck130_assertion evidence source_evidence_literature NP887369.RABcikVSVUirR10WxW7ARBkY3373p7skFupYL1vSjKvck130_provenance.
- NP887369.RABcikVSVUirR10WxW7ARBkY3373p7skFupYL1vSjKvck130_assertion SIO_000772 21496327 NP887369.RABcikVSVUirR10WxW7ARBkY3373p7skFupYL1vSjKvck130_provenance.
- NP887369.RABcikVSVUirR10WxW7ARBkY3373p7skFupYL1vSjKvck130_assertion wasDerivedFrom befree-2016 NP887369.RABcikVSVUirR10WxW7ARBkY3373p7skFupYL1vSjKvck130_provenance.
- NP887369.RABcikVSVUirR10WxW7ARBkY3373p7skFupYL1vSjKvck130_assertion wasGeneratedBy ECO_0000203 NP887369.RABcikVSVUirR10WxW7ARBkY3373p7skFupYL1vSjKvck130_provenance.
- befree-2016 importedOn "2016-02-19" NP887369.RABcikVSVUirR10WxW7ARBkY3373p7skFupYL1vSjKvck130_provenance.