Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP916932.RAaNcEAYBuXSzy4HA3JC4sz9K6Da04qOWczFYGeycT6Sc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP916932.RAaNcEAYBuXSzy4HA3JC4sz9K6Da04qOWczFYGeycT6Sc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP916932.RAaNcEAYBuXSzy4HA3JC4sz9K6Da04qOWczFYGeycT6Sc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP916932.RAaNcEAYBuXSzy4HA3JC4sz9K6Da04qOWczFYGeycT6Sc130_provenance.
- NP916932.RAaNcEAYBuXSzy4HA3JC4sz9K6Da04qOWczFYGeycT6Sc130_assertion description "[No associations were found between IL1B C(-31)T or IL1RN VNTR genotypes, alleles or haplotypes and the severity of CAD when subgroups with SVD and MVD were compared.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916932.RAaNcEAYBuXSzy4HA3JC4sz9K6Da04qOWczFYGeycT6Sc130_provenance.
- NP916932.RAaNcEAYBuXSzy4HA3JC4sz9K6Da04qOWczFYGeycT6Sc130_assertion evidence source_evidence_literature NP916932.RAaNcEAYBuXSzy4HA3JC4sz9K6Da04qOWczFYGeycT6Sc130_provenance.
- NP916932.RAaNcEAYBuXSzy4HA3JC4sz9K6Da04qOWczFYGeycT6Sc130_assertion SIO_000772 21840356 NP916932.RAaNcEAYBuXSzy4HA3JC4sz9K6Da04qOWczFYGeycT6Sc130_provenance.
- NP916932.RAaNcEAYBuXSzy4HA3JC4sz9K6Da04qOWczFYGeycT6Sc130_assertion wasDerivedFrom befree-2016 NP916932.RAaNcEAYBuXSzy4HA3JC4sz9K6Da04qOWczFYGeycT6Sc130_provenance.
- NP916932.RAaNcEAYBuXSzy4HA3JC4sz9K6Da04qOWczFYGeycT6Sc130_assertion wasGeneratedBy ECO_0000203 NP916932.RAaNcEAYBuXSzy4HA3JC4sz9K6Da04qOWczFYGeycT6Sc130_provenance.
- befree-2016 importedOn "2016-02-19" NP916932.RAaNcEAYBuXSzy4HA3JC4sz9K6Da04qOWczFYGeycT6Sc130_provenance.