Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP141014.RABMPnw6lRlUWzoBQlR_ajg4PiKa_vxoTe6WC353oFMUs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP141014.RABMPnw6lRlUWzoBQlR_ajg4PiKa_vxoTe6WC353oFMUs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP141014.RABMPnw6lRlUWzoBQlR_ajg4PiKa_vxoTe6WC353oFMUs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP141014.RABMPnw6lRlUWzoBQlR_ajg4PiKa_vxoTe6WC353oFMUs130_provenance.
- NP141014.RABMPnw6lRlUWzoBQlR_ajg4PiKa_vxoTe6WC353oFMUs130_assertion description "[Suggested as a candidate gene for a dominant syndrome that consists of inclusion body myopathy, Paget disease of bone, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141014.RABMPnw6lRlUWzoBQlR_ajg4PiKa_vxoTe6WC353oFMUs130_provenance.
- NP141014.RABMPnw6lRlUWzoBQlR_ajg4PiKa_vxoTe6WC353oFMUs130_assertion evidence source_evidence_literature NP141014.RABMPnw6lRlUWzoBQlR_ajg4PiKa_vxoTe6WC353oFMUs130_provenance.
- NP141014.RABMPnw6lRlUWzoBQlR_ajg4PiKa_vxoTe6WC353oFMUs130_assertion SIO_000772 11749051 NP141014.RABMPnw6lRlUWzoBQlR_ajg4PiKa_vxoTe6WC353oFMUs130_provenance.
- NP141014.RABMPnw6lRlUWzoBQlR_ajg4PiKa_vxoTe6WC353oFMUs130_assertion wasDerivedFrom lhgdn-20090331 NP141014.RABMPnw6lRlUWzoBQlR_ajg4PiKa_vxoTe6WC353oFMUs130_provenance.
- NP141014.RABMPnw6lRlUWzoBQlR_ajg4PiKa_vxoTe6WC353oFMUs130_assertion wasGeneratedBy ECO_0000203 NP141014.RABMPnw6lRlUWzoBQlR_ajg4PiKa_vxoTe6WC353oFMUs130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP141014.RABMPnw6lRlUWzoBQlR_ajg4PiKa_vxoTe6WC353oFMUs130_provenance.