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- source_evidence_literature type ECO_0000212 NP372497.RAuzmKJcy-1msLdzD8UUEYOLHrNLGGzSlEXHg86t7FeJ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP372497.RAuzmKJcy-1msLdzD8UUEYOLHrNLGGzSlEXHg86t7FeJ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP372497.RAuzmKJcy-1msLdzD8UUEYOLHrNLGGzSlEXHg86t7FeJ0130_provenance.
- NP372497.RAuzmKJcy-1msLdzD8UUEYOLHrNLGGzSlEXHg86t7FeJ0130_assertion description "[Inclusion body myopathy with Paget disease of the bone (PDB) and/or frontotemporal dementia (IBMPFD, OMIM 167320), is a progressive autosomal dominant disorder caused by mutations in the Valousin-containing protein (VCP, p97 or CDC48) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372497.RAuzmKJcy-1msLdzD8UUEYOLHrNLGGzSlEXHg86t7FeJ0130_provenance.
- NP372497.RAuzmKJcy-1msLdzD8UUEYOLHrNLGGzSlEXHg86t7FeJ0130_assertion evidence source_evidence_literature NP372497.RAuzmKJcy-1msLdzD8UUEYOLHrNLGGzSlEXHg86t7FeJ0130_provenance.
- NP372497.RAuzmKJcy-1msLdzD8UUEYOLHrNLGGzSlEXHg86t7FeJ0130_assertion SIO_000772 18260132 NP372497.RAuzmKJcy-1msLdzD8UUEYOLHrNLGGzSlEXHg86t7FeJ0130_provenance.
- NP372497.RAuzmKJcy-1msLdzD8UUEYOLHrNLGGzSlEXHg86t7FeJ0130_assertion wasDerivedFrom befree-20150227 NP372497.RAuzmKJcy-1msLdzD8UUEYOLHrNLGGzSlEXHg86t7FeJ0130_provenance.
- NP372497.RAuzmKJcy-1msLdzD8UUEYOLHrNLGGzSlEXHg86t7FeJ0130_assertion wasGeneratedBy ECO_0000203 NP372497.RAuzmKJcy-1msLdzD8UUEYOLHrNLGGzSlEXHg86t7FeJ0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP372497.RAuzmKJcy-1msLdzD8UUEYOLHrNLGGzSlEXHg86t7FeJ0130_provenance.