Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP171843.RA8Of6Dh26TRfOVRQ97keLi5J8XE0hxfZjgTQeB6lPEGc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP171843.RA8Of6Dh26TRfOVRQ97keLi5J8XE0hxfZjgTQeB6lPEGc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP171843.RA8Of6Dh26TRfOVRQ97keLi5J8XE0hxfZjgTQeB6lPEGc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP171843.RA8Of6Dh26TRfOVRQ97keLi5J8XE0hxfZjgTQeB6lPEGc130_provenance.
- NP171843.RA8Of6Dh26TRfOVRQ97keLi5J8XE0hxfZjgTQeB6lPEGc130_assertion description "[Complete loss of expression of the ANT1 gene causes a clinical syndrome mainly characterised by cardiomyopathy and myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP171843.RA8Of6Dh26TRfOVRQ97keLi5J8XE0hxfZjgTQeB6lPEGc130_provenance.
- NP171843.RA8Of6Dh26TRfOVRQ97keLi5J8XE0hxfZjgTQeB6lPEGc130_assertion evidence source_evidence_literature NP171843.RA8Of6Dh26TRfOVRQ97keLi5J8XE0hxfZjgTQeB6lPEGc130_provenance.
- NP171843.RA8Of6Dh26TRfOVRQ97keLi5J8XE0hxfZjgTQeB6lPEGc130_assertion SIO_000772 22187496 NP171843.RA8Of6Dh26TRfOVRQ97keLi5J8XE0hxfZjgTQeB6lPEGc130_provenance.
- NP171843.RA8Of6Dh26TRfOVRQ97keLi5J8XE0hxfZjgTQeB6lPEGc130_assertion wasDerivedFrom befree-20140225 NP171843.RA8Of6Dh26TRfOVRQ97keLi5J8XE0hxfZjgTQeB6lPEGc130_provenance.
- NP171843.RA8Of6Dh26TRfOVRQ97keLi5J8XE0hxfZjgTQeB6lPEGc130_assertion wasGeneratedBy ECO_0000203 NP171843.RA8Of6Dh26TRfOVRQ97keLi5J8XE0hxfZjgTQeB6lPEGc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP171843.RA8Of6Dh26TRfOVRQ97keLi5J8XE0hxfZjgTQeB6lPEGc130_provenance.