Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP620336.RAZhhuXRk0TEBVGTyNaLH4mDiUYqjVJXBlMD_1L4saK-E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP620336.RAZhhuXRk0TEBVGTyNaLH4mDiUYqjVJXBlMD_1L4saK-E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP620336.RAZhhuXRk0TEBVGTyNaLH4mDiUYqjVJXBlMD_1L4saK-E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP620336.RAZhhuXRk0TEBVGTyNaLH4mDiUYqjVJXBlMD_1L4saK-E130_provenance.
- NP620336.RAZhhuXRk0TEBVGTyNaLH4mDiUYqjVJXBlMD_1L4saK-E130_assertion description "[We investigated haemorheological variables in patients with idiopathic sudden sensorineural hearing loss (ISSHL), retinal vein occlusion (RVO) and systemic sclerosis (SSc), as possible models of microvascular damage, and their relationship with eNOS gene T-786C, G894T and 4a/4b polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP620336.RAZhhuXRk0TEBVGTyNaLH4mDiUYqjVJXBlMD_1L4saK-E130_provenance.
- NP620336.RAZhhuXRk0TEBVGTyNaLH4mDiUYqjVJXBlMD_1L4saK-E130_assertion evidence source_evidence_literature NP620336.RAZhhuXRk0TEBVGTyNaLH4mDiUYqjVJXBlMD_1L4saK-E130_provenance.
- NP620336.RAZhhuXRk0TEBVGTyNaLH4mDiUYqjVJXBlMD_1L4saK-E130_assertion SIO_000772 17634663 NP620336.RAZhhuXRk0TEBVGTyNaLH4mDiUYqjVJXBlMD_1L4saK-E130_provenance.
- NP620336.RAZhhuXRk0TEBVGTyNaLH4mDiUYqjVJXBlMD_1L4saK-E130_assertion wasDerivedFrom befree-2016 NP620336.RAZhhuXRk0TEBVGTyNaLH4mDiUYqjVJXBlMD_1L4saK-E130_provenance.
- NP620336.RAZhhuXRk0TEBVGTyNaLH4mDiUYqjVJXBlMD_1L4saK-E130_assertion wasGeneratedBy ECO_0000203 NP620336.RAZhhuXRk0TEBVGTyNaLH4mDiUYqjVJXBlMD_1L4saK-E130_provenance.
- befree-2016 importedOn "2016-02-19" NP620336.RAZhhuXRk0TEBVGTyNaLH4mDiUYqjVJXBlMD_1L4saK-E130_provenance.