Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP196648.RAuoGd2VRioVFpv-b77JpUft144qrYq21nEaGniG6_aEg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP196648.RAuoGd2VRioVFpv-b77JpUft144qrYq21nEaGniG6_aEg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP196648.RAuoGd2VRioVFpv-b77JpUft144qrYq21nEaGniG6_aEg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP196648.RAuoGd2VRioVFpv-b77JpUft144qrYq21nEaGniG6_aEg130_provenance.
- NP196648.RAuoGd2VRioVFpv-b77JpUft144qrYq21nEaGniG6_aEg130_assertion description "[calsequestrin 2 mutations causes severe forms of catecholaminergic polymorphic ventricular tachycardia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP196648.RAuoGd2VRioVFpv-b77JpUft144qrYq21nEaGniG6_aEg130_provenance.
- NP196648.RAuoGd2VRioVFpv-b77JpUft144qrYq21nEaGniG6_aEg130_assertion evidence source_evidence_literature NP196648.RAuoGd2VRioVFpv-b77JpUft144qrYq21nEaGniG6_aEg130_provenance.
- NP196648.RAuoGd2VRioVFpv-b77JpUft144qrYq21nEaGniG6_aEg130_assertion SIO_000772 12386154 NP196648.RAuoGd2VRioVFpv-b77JpUft144qrYq21nEaGniG6_aEg130_provenance.
- NP196648.RAuoGd2VRioVFpv-b77JpUft144qrYq21nEaGniG6_aEg130_assertion wasDerivedFrom lhgdn-20090331 NP196648.RAuoGd2VRioVFpv-b77JpUft144qrYq21nEaGniG6_aEg130_provenance.
- NP196648.RAuoGd2VRioVFpv-b77JpUft144qrYq21nEaGniG6_aEg130_assertion wasGeneratedBy ECO_0000203 NP196648.RAuoGd2VRioVFpv-b77JpUft144qrYq21nEaGniG6_aEg130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP196648.RAuoGd2VRioVFpv-b77JpUft144qrYq21nEaGniG6_aEg130_provenance.