Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1246713.RAPX3Wi4liGuVN8HTAoNUpFB91WggY_2GY3UY8TSm8mys130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1246713.RAPX3Wi4liGuVN8HTAoNUpFB91WggY_2GY3UY8TSm8mys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246713.RAPX3Wi4liGuVN8HTAoNUpFB91WggY_2GY3UY8TSm8mys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246713.RAPX3Wi4liGuVN8HTAoNUpFB91WggY_2GY3UY8TSm8mys130_provenance.
- NP1246713.RAPX3Wi4liGuVN8HTAoNUpFB91WggY_2GY3UY8TSm8mys130_assertion description "[The coexistence of dynamin 2 mutation and multiple mitochondrial DNA (mtDNA) deletions in the background of severe cardiomyopathy and centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246713.RAPX3Wi4liGuVN8HTAoNUpFB91WggY_2GY3UY8TSm8mys130_provenance.
- NP1246713.RAPX3Wi4liGuVN8HTAoNUpFB91WggY_2GY3UY8TSm8mys130_assertion evidence source_evidence_literature NP1246713.RAPX3Wi4liGuVN8HTAoNUpFB91WggY_2GY3UY8TSm8mys130_provenance.
- NP1246713.RAPX3Wi4liGuVN8HTAoNUpFB91WggY_2GY3UY8TSm8mys130_assertion SIO_000772 25492887 NP1246713.RAPX3Wi4liGuVN8HTAoNUpFB91WggY_2GY3UY8TSm8mys130_provenance.
- NP1246713.RAPX3Wi4liGuVN8HTAoNUpFB91WggY_2GY3UY8TSm8mys130_assertion wasDerivedFrom befree-2016 NP1246713.RAPX3Wi4liGuVN8HTAoNUpFB91WggY_2GY3UY8TSm8mys130_provenance.
- NP1246713.RAPX3Wi4liGuVN8HTAoNUpFB91WggY_2GY3UY8TSm8mys130_assertion wasGeneratedBy ECO_0000203 NP1246713.RAPX3Wi4liGuVN8HTAoNUpFB91WggY_2GY3UY8TSm8mys130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246713.RAPX3Wi4liGuVN8HTAoNUpFB91WggY_2GY3UY8TSm8mys130_provenance.