Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1242240.RAe-bArRnpid85yIGQRA62AIqmNkk01GKl1s3GNCaLXso130_assertion> ?p ?o ?g. }
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- NP1242240.RAe-bArRnpid85yIGQRA62AIqmNkk01GKl1s3GNCaLXso130_assertion type Assertion NP1242240.RAe-bArRnpid85yIGQRA62AIqmNkk01GKl1s3GNCaLXso130_head.
- NP1242240.RAe-bArRnpid85yIGQRA62AIqmNkk01GKl1s3GNCaLXso130_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." NP1242240.RAe-bArRnpid85yIGQRA62AIqmNkk01GKl1s3GNCaLXso130_provenance.
- NP1242240.RAe-bArRnpid85yIGQRA62AIqmNkk01GKl1s3GNCaLXso130_assertion evidence source_evidence_literature NP1242240.RAe-bArRnpid85yIGQRA62AIqmNkk01GKl1s3GNCaLXso130_provenance.
- NP1242240.RAe-bArRnpid85yIGQRA62AIqmNkk01GKl1s3GNCaLXso130_assertion SIO_000772 25447673 NP1242240.RAe-bArRnpid85yIGQRA62AIqmNkk01GKl1s3GNCaLXso130_provenance.
- NP1242240.RAe-bArRnpid85yIGQRA62AIqmNkk01GKl1s3GNCaLXso130_assertion wasDerivedFrom befree-2016 NP1242240.RAe-bArRnpid85yIGQRA62AIqmNkk01GKl1s3GNCaLXso130_provenance.
- NP1242240.RAe-bArRnpid85yIGQRA62AIqmNkk01GKl1s3GNCaLXso130_assertion wasGeneratedBy ECO_0000203 NP1242240.RAe-bArRnpid85yIGQRA62AIqmNkk01GKl1s3GNCaLXso130_provenance.