Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP566208.RAIsSE2wMyxbQSwZLh1daxx-7l09fSswpQPSMeq3m-QIo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP566208.RAIsSE2wMyxbQSwZLh1daxx-7l09fSswpQPSMeq3m-QIo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP566208.RAIsSE2wMyxbQSwZLh1daxx-7l09fSswpQPSMeq3m-QIo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP566208.RAIsSE2wMyxbQSwZLh1daxx-7l09fSswpQPSMeq3m-QIo130_provenance.
- NP566208.RAIsSE2wMyxbQSwZLh1daxx-7l09fSswpQPSMeq3m-QIo130_assertion description "[We genotyped five polymorphisms of the AGT, ACE, AT1R, 5-HT2A, and 5-HTT genes in 245 patients with Hypertrophic Cardiomyopathy (HCM; 205 without an identified sarcomeric gene mutation), in 145 patients with LVH secondary to hypertension, and 300 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP566208.RAIsSE2wMyxbQSwZLh1daxx-7l09fSswpQPSMeq3m-QIo130_provenance.
- NP566208.RAIsSE2wMyxbQSwZLh1daxx-7l09fSswpQPSMeq3m-QIo130_assertion evidence source_evidence_literature NP566208.RAIsSE2wMyxbQSwZLh1daxx-7l09fSswpQPSMeq3m-QIo130_provenance.
- NP566208.RAIsSE2wMyxbQSwZLh1daxx-7l09fSswpQPSMeq3m-QIo130_assertion SIO_000772 20594303 NP566208.RAIsSE2wMyxbQSwZLh1daxx-7l09fSswpQPSMeq3m-QIo130_provenance.
- NP566208.RAIsSE2wMyxbQSwZLh1daxx-7l09fSswpQPSMeq3m-QIo130_assertion wasDerivedFrom befree-20140225 NP566208.RAIsSE2wMyxbQSwZLh1daxx-7l09fSswpQPSMeq3m-QIo130_provenance.
- NP566208.RAIsSE2wMyxbQSwZLh1daxx-7l09fSswpQPSMeq3m-QIo130_assertion wasGeneratedBy ECO_0000203 NP566208.RAIsSE2wMyxbQSwZLh1daxx-7l09fSswpQPSMeq3m-QIo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP566208.RAIsSE2wMyxbQSwZLh1daxx-7l09fSswpQPSMeq3m-QIo130_provenance.