Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP797364.RAHvxXJPoyQGF0-jRBEgr2BbRK8ek-qU-NLAuyMJ-shA0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP797364.RAHvxXJPoyQGF0-jRBEgr2BbRK8ek-qU-NLAuyMJ-shA0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP797364.RAHvxXJPoyQGF0-jRBEgr2BbRK8ek-qU-NLAuyMJ-shA0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP797364.RAHvxXJPoyQGF0-jRBEgr2BbRK8ek-qU-NLAuyMJ-shA0130_provenance.
- NP797364.RAHvxXJPoyQGF0-jRBEgr2BbRK8ek-qU-NLAuyMJ-shA0130_assertion description "[Genotypes for ERLIN1, TRAPPC9, and WNK2 may prove informative for assessment of the genetic risk for intracerebral hemorrhage, and those for ITM2C and MAPKAP1 may be beneficial in assessment of the genetic risk for subarachnoid hemorrhage in Japanese individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP797364.RAHvxXJPoyQGF0-jRBEgr2BbRK8ek-qU-NLAuyMJ-shA0130_provenance.
- NP797364.RAHvxXJPoyQGF0-jRBEgr2BbRK8ek-qU-NLAuyMJ-shA0130_assertion evidence source_evidence_literature NP797364.RAHvxXJPoyQGF0-jRBEgr2BbRK8ek-qU-NLAuyMJ-shA0130_provenance.
- NP797364.RAHvxXJPoyQGF0-jRBEgr2BbRK8ek-qU-NLAuyMJ-shA0130_assertion SIO_000772 20198315 NP797364.RAHvxXJPoyQGF0-jRBEgr2BbRK8ek-qU-NLAuyMJ-shA0130_provenance.
- NP797364.RAHvxXJPoyQGF0-jRBEgr2BbRK8ek-qU-NLAuyMJ-shA0130_assertion wasDerivedFrom befree-2016 NP797364.RAHvxXJPoyQGF0-jRBEgr2BbRK8ek-qU-NLAuyMJ-shA0130_provenance.
- NP797364.RAHvxXJPoyQGF0-jRBEgr2BbRK8ek-qU-NLAuyMJ-shA0130_assertion wasGeneratedBy ECO_0000203 NP797364.RAHvxXJPoyQGF0-jRBEgr2BbRK8ek-qU-NLAuyMJ-shA0130_provenance.
- befree-2016 importedOn "2016-02-19" NP797364.RAHvxXJPoyQGF0-jRBEgr2BbRK8ek-qU-NLAuyMJ-shA0130_provenance.