Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP914478.RAA0SUEcpCD_C2SMtu-tPsbA50x-KtKBfxX9sd3QBpwJc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914478.RAA0SUEcpCD_C2SMtu-tPsbA50x-KtKBfxX9sd3QBpwJc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914478.RAA0SUEcpCD_C2SMtu-tPsbA50x-KtKBfxX9sd3QBpwJc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914478.RAA0SUEcpCD_C2SMtu-tPsbA50x-KtKBfxX9sd3QBpwJc130_provenance.
- NP914478.RAA0SUEcpCD_C2SMtu-tPsbA50x-KtKBfxX9sd3QBpwJc130_assertion description "[Emery-Dreifuss muscular dystrophy, caused by EMD gene mutations, is characterized by humeroperoneal muscular dystrophy, joint contractures, and conduction defects and is often associated with sudden cardiac death, even without prior cardiac symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914478.RAA0SUEcpCD_C2SMtu-tPsbA50x-KtKBfxX9sd3QBpwJc130_provenance.
- NP914478.RAA0SUEcpCD_C2SMtu-tPsbA50x-KtKBfxX9sd3QBpwJc130_assertion evidence source_evidence_literature NP914478.RAA0SUEcpCD_C2SMtu-tPsbA50x-KtKBfxX9sd3QBpwJc130_provenance.
- NP914478.RAA0SUEcpCD_C2SMtu-tPsbA50x-KtKBfxX9sd3QBpwJc130_assertion SIO_000772 17620497 NP914478.RAA0SUEcpCD_C2SMtu-tPsbA50x-KtKBfxX9sd3QBpwJc130_provenance.
- NP914478.RAA0SUEcpCD_C2SMtu-tPsbA50x-KtKBfxX9sd3QBpwJc130_assertion wasDerivedFrom befree-20140225 NP914478.RAA0SUEcpCD_C2SMtu-tPsbA50x-KtKBfxX9sd3QBpwJc130_provenance.
- NP914478.RAA0SUEcpCD_C2SMtu-tPsbA50x-KtKBfxX9sd3QBpwJc130_assertion wasGeneratedBy ECO_0000203 NP914478.RAA0SUEcpCD_C2SMtu-tPsbA50x-KtKBfxX9sd3QBpwJc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP914478.RAA0SUEcpCD_C2SMtu-tPsbA50x-KtKBfxX9sd3QBpwJc130_provenance.