Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP269398.RA5dfLHzFyIj57fljKfuam-Q20Bz3BQl5RIEJA2VOBlHk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP269398.RA5dfLHzFyIj57fljKfuam-Q20Bz3BQl5RIEJA2VOBlHk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP269398.RA5dfLHzFyIj57fljKfuam-Q20Bz3BQl5RIEJA2VOBlHk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP269398.RA5dfLHzFyIj57fljKfuam-Q20Bz3BQl5RIEJA2VOBlHk130_provenance.
- NP269398.RA5dfLHzFyIj57fljKfuam-Q20Bz3BQl5RIEJA2VOBlHk130_assertion description "[Mutations in the valosin-containing protein (VCP) gene on chromosome 9p13-p12 recently have been shown to cause autosomal dominant inclusion body myopathy associated with Paget's disease of the bone and frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269398.RA5dfLHzFyIj57fljKfuam-Q20Bz3BQl5RIEJA2VOBlHk130_provenance.
- NP269398.RA5dfLHzFyIj57fljKfuam-Q20Bz3BQl5RIEJA2VOBlHk130_assertion evidence source_evidence_literature NP269398.RA5dfLHzFyIj57fljKfuam-Q20Bz3BQl5RIEJA2VOBlHk130_provenance.
- NP269398.RA5dfLHzFyIj57fljKfuam-Q20Bz3BQl5RIEJA2VOBlHk130_assertion SIO_000772 15732117 NP269398.RA5dfLHzFyIj57fljKfuam-Q20Bz3BQl5RIEJA2VOBlHk130_provenance.
- NP269398.RA5dfLHzFyIj57fljKfuam-Q20Bz3BQl5RIEJA2VOBlHk130_assertion wasDerivedFrom befree-20140225 NP269398.RA5dfLHzFyIj57fljKfuam-Q20Bz3BQl5RIEJA2VOBlHk130_provenance.
- NP269398.RA5dfLHzFyIj57fljKfuam-Q20Bz3BQl5RIEJA2VOBlHk130_assertion wasGeneratedBy ECO_0000203 NP269398.RA5dfLHzFyIj57fljKfuam-Q20Bz3BQl5RIEJA2VOBlHk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP269398.RA5dfLHzFyIj57fljKfuam-Q20Bz3BQl5RIEJA2VOBlHk130_provenance.