Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP699626.RAvsUGcgpjBZJa7OLgeLblBWUFxX9qNytV1fW8WQPd8oI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP699626.RAvsUGcgpjBZJa7OLgeLblBWUFxX9qNytV1fW8WQPd8oI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP699626.RAvsUGcgpjBZJa7OLgeLblBWUFxX9qNytV1fW8WQPd8oI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP699626.RAvsUGcgpjBZJa7OLgeLblBWUFxX9qNytV1fW8WQPd8oI130_provenance.
- NP699626.RAvsUGcgpjBZJa7OLgeLblBWUFxX9qNytV1fW8WQPd8oI130_assertion description "[In white CHS participants, the prespecified risk alleles of 7 of the 74 SNPs (in HPS1, ITGAE, ABCG2, MYH15, FSTL4, CALM1, and BAT2) were nominally associated with increased risk of stroke (one-sided P<0.05, false discovery rate=0.42).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699626.RAvsUGcgpjBZJa7OLgeLblBWUFxX9qNytV1fW8WQPd8oI130_provenance.
- NP699626.RAvsUGcgpjBZJa7OLgeLblBWUFxX9qNytV1fW8WQPd8oI130_assertion evidence source_evidence_literature NP699626.RAvsUGcgpjBZJa7OLgeLblBWUFxX9qNytV1fW8WQPd8oI130_provenance.
- NP699626.RAvsUGcgpjBZJa7OLgeLblBWUFxX9qNytV1fW8WQPd8oI130_assertion SIO_000772 19023099 NP699626.RAvsUGcgpjBZJa7OLgeLblBWUFxX9qNytV1fW8WQPd8oI130_provenance.
- NP699626.RAvsUGcgpjBZJa7OLgeLblBWUFxX9qNytV1fW8WQPd8oI130_assertion wasDerivedFrom befree-20140225 NP699626.RAvsUGcgpjBZJa7OLgeLblBWUFxX9qNytV1fW8WQPd8oI130_provenance.
- NP699626.RAvsUGcgpjBZJa7OLgeLblBWUFxX9qNytV1fW8WQPd8oI130_assertion wasGeneratedBy ECO_0000203 NP699626.RAvsUGcgpjBZJa7OLgeLblBWUFxX9qNytV1fW8WQPd8oI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP699626.RAvsUGcgpjBZJa7OLgeLblBWUFxX9qNytV1fW8WQPd8oI130_provenance.