Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP171914.RABX938BfLENCQHluZlSjiFn6mcX63UqMBh3GG0QGNiTw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP171914.RABX938BfLENCQHluZlSjiFn6mcX63UqMBh3GG0QGNiTw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP171914.RABX938BfLENCQHluZlSjiFn6mcX63UqMBh3GG0QGNiTw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP171914.RABX938BfLENCQHluZlSjiFn6mcX63UqMBh3GG0QGNiTw130_provenance.
- NP171914.RABX938BfLENCQHluZlSjiFn6mcX63UqMBh3GG0QGNiTw130_assertion description "[Located within the minimum VCPDM candidate interval, myotilin mutations also cause a similarly progressive and adult-onset muscle disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP171914.RABX938BfLENCQHluZlSjiFn6mcX63UqMBh3GG0QGNiTw130_provenance.
- NP171914.RABX938BfLENCQHluZlSjiFn6mcX63UqMBh3GG0QGNiTw130_assertion evidence source_evidence_literature NP171914.RABX938BfLENCQHluZlSjiFn6mcX63UqMBh3GG0QGNiTw130_provenance.
- NP171914.RABX938BfLENCQHluZlSjiFn6mcX63UqMBh3GG0QGNiTw130_assertion SIO_000772 16674563 NP171914.RABX938BfLENCQHluZlSjiFn6mcX63UqMBh3GG0QGNiTw130_provenance.
- NP171914.RABX938BfLENCQHluZlSjiFn6mcX63UqMBh3GG0QGNiTw130_assertion wasDerivedFrom befree-20140225 NP171914.RABX938BfLENCQHluZlSjiFn6mcX63UqMBh3GG0QGNiTw130_provenance.
- NP171914.RABX938BfLENCQHluZlSjiFn6mcX63UqMBh3GG0QGNiTw130_assertion wasGeneratedBy ECO_0000203 NP171914.RABX938BfLENCQHluZlSjiFn6mcX63UqMBh3GG0QGNiTw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP171914.RABX938BfLENCQHluZlSjiFn6mcX63UqMBh3GG0QGNiTw130_provenance.