Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP146499.RAmF8FsP62zOavmL9ArcAC2DMw47FNJEWZ_-nOSOAUFRM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP146499.RAmF8FsP62zOavmL9ArcAC2DMw47FNJEWZ_-nOSOAUFRM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP146499.RAmF8FsP62zOavmL9ArcAC2DMw47FNJEWZ_-nOSOAUFRM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP146499.RAmF8FsP62zOavmL9ArcAC2DMw47FNJEWZ_-nOSOAUFRM130_provenance.
- NP146499.RAmF8FsP62zOavmL9ArcAC2DMw47FNJEWZ_-nOSOAUFRM130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146499.RAmF8FsP62zOavmL9ArcAC2DMw47FNJEWZ_-nOSOAUFRM130_provenance.
- NP146499.RAmF8FsP62zOavmL9ArcAC2DMw47FNJEWZ_-nOSOAUFRM130_assertion evidence source_evidence_literature NP146499.RAmF8FsP62zOavmL9ArcAC2DMw47FNJEWZ_-nOSOAUFRM130_provenance.
- NP146499.RAmF8FsP62zOavmL9ArcAC2DMw47FNJEWZ_-nOSOAUFRM130_assertion SIO_000772 19412328 NP146499.RAmF8FsP62zOavmL9ArcAC2DMw47FNJEWZ_-nOSOAUFRM130_provenance.
- NP146499.RAmF8FsP62zOavmL9ArcAC2DMw47FNJEWZ_-nOSOAUFRM130_assertion wasDerivedFrom gad-20150221 NP146499.RAmF8FsP62zOavmL9ArcAC2DMw47FNJEWZ_-nOSOAUFRM130_provenance.
- NP146499.RAmF8FsP62zOavmL9ArcAC2DMw47FNJEWZ_-nOSOAUFRM130_assertion wasGeneratedBy ECO_0000203 NP146499.RAmF8FsP62zOavmL9ArcAC2DMw47FNJEWZ_-nOSOAUFRM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP146499.RAmF8FsP62zOavmL9ArcAC2DMw47FNJEWZ_-nOSOAUFRM130_provenance.