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- source_evidence_literature type ECO_0000212 NP768742.RAfLU7O-Yq0m2sg55QgRJvTbUYJdppLiatB3CRkgXHONE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768742.RAfLU7O-Yq0m2sg55QgRJvTbUYJdppLiatB3CRkgXHONE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768742.RAfLU7O-Yq0m2sg55QgRJvTbUYJdppLiatB3CRkgXHONE130_provenance.
- NP768742.RAfLU7O-Yq0m2sg55QgRJvTbUYJdppLiatB3CRkgXHONE130_assertion description "[A genetic deficiency of VCP can cause inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768742.RAfLU7O-Yq0m2sg55QgRJvTbUYJdppLiatB3CRkgXHONE130_provenance.
- NP768742.RAfLU7O-Yq0m2sg55QgRJvTbUYJdppLiatB3CRkgXHONE130_assertion evidence source_evidence_literature NP768742.RAfLU7O-Yq0m2sg55QgRJvTbUYJdppLiatB3CRkgXHONE130_provenance.
- NP768742.RAfLU7O-Yq0m2sg55QgRJvTbUYJdppLiatB3CRkgXHONE130_assertion SIO_000772 25447673 NP768742.RAfLU7O-Yq0m2sg55QgRJvTbUYJdppLiatB3CRkgXHONE130_provenance.
- NP768742.RAfLU7O-Yq0m2sg55QgRJvTbUYJdppLiatB3CRkgXHONE130_assertion wasDerivedFrom befree-20150227 NP768742.RAfLU7O-Yq0m2sg55QgRJvTbUYJdppLiatB3CRkgXHONE130_provenance.
- NP768742.RAfLU7O-Yq0m2sg55QgRJvTbUYJdppLiatB3CRkgXHONE130_assertion wasGeneratedBy ECO_0000203 NP768742.RAfLU7O-Yq0m2sg55QgRJvTbUYJdppLiatB3CRkgXHONE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP768742.RAfLU7O-Yq0m2sg55QgRJvTbUYJdppLiatB3CRkgXHONE130_provenance.