Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP420700.RAgyrRB1yh0xtPeEdb1YyyEfKx0U6BYu_NjSX9s3OH88Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP420700.RAgyrRB1yh0xtPeEdb1YyyEfKx0U6BYu_NjSX9s3OH88Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420700.RAgyrRB1yh0xtPeEdb1YyyEfKx0U6BYu_NjSX9s3OH88Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420700.RAgyrRB1yh0xtPeEdb1YyyEfKx0U6BYu_NjSX9s3OH88Y130_provenance.
- NP420700.RAgyrRB1yh0xtPeEdb1YyyEfKx0U6BYu_NjSX9s3OH88Y130_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." NP420700.RAgyrRB1yh0xtPeEdb1YyyEfKx0U6BYu_NjSX9s3OH88Y130_provenance.
- NP420700.RAgyrRB1yh0xtPeEdb1YyyEfKx0U6BYu_NjSX9s3OH88Y130_assertion evidence source_evidence_literature NP420700.RAgyrRB1yh0xtPeEdb1YyyEfKx0U6BYu_NjSX9s3OH88Y130_provenance.
- NP420700.RAgyrRB1yh0xtPeEdb1YyyEfKx0U6BYu_NjSX9s3OH88Y130_assertion SIO_000772 15732117 NP420700.RAgyrRB1yh0xtPeEdb1YyyEfKx0U6BYu_NjSX9s3OH88Y130_provenance.
- NP420700.RAgyrRB1yh0xtPeEdb1YyyEfKx0U6BYu_NjSX9s3OH88Y130_assertion wasDerivedFrom befree-20140225 NP420700.RAgyrRB1yh0xtPeEdb1YyyEfKx0U6BYu_NjSX9s3OH88Y130_provenance.
- NP420700.RAgyrRB1yh0xtPeEdb1YyyEfKx0U6BYu_NjSX9s3OH88Y130_assertion wasGeneratedBy ECO_0000203 NP420700.RAgyrRB1yh0xtPeEdb1YyyEfKx0U6BYu_NjSX9s3OH88Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP420700.RAgyrRB1yh0xtPeEdb1YyyEfKx0U6BYu_NjSX9s3OH88Y130_provenance.