Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP224571.RAaJiZGMY37lzId43O94l72pMf9XaRR92veZcjjkdtF4w130_assertion> ?p ?o ?g. }
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- NP224571.RAaJiZGMY37lzId43O94l72pMf9XaRR92veZcjjkdtF4w130_assertion type Assertion NP224571.RAaJiZGMY37lzId43O94l72pMf9XaRR92veZcjjkdtF4w130_head.
- NP224571.RAaJiZGMY37lzId43O94l72pMf9XaRR92veZcjjkdtF4w130_assertion wasGeneratedBy ECO_0000203 NP224571.RAaJiZGMY37lzId43O94l72pMf9XaRR92veZcjjkdtF4w130_provenance.
- NP224571.RAaJiZGMY37lzId43O94l72pMf9XaRR92veZcjjkdtF4w130_assertion wasDerivedFrom lhgdn-20090331 NP224571.RAaJiZGMY37lzId43O94l72pMf9XaRR92veZcjjkdtF4w130_provenance.
- NP224571.RAaJiZGMY37lzId43O94l72pMf9XaRR92veZcjjkdtF4w130_assertion SIO_000772 17457594 NP224571.RAaJiZGMY37lzId43O94l72pMf9XaRR92veZcjjkdtF4w130_provenance.
- NP224571.RAaJiZGMY37lzId43O94l72pMf9XaRR92veZcjjkdtF4w130_assertion evidence source_evidence_literature NP224571.RAaJiZGMY37lzId43O94l72pMf9XaRR92veZcjjkdtF4w130_provenance.
- NP224571.RAaJiZGMY37lzId43O94l72pMf9XaRR92veZcjjkdtF4w130_assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) is a rare, autosomal dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP224571.RAaJiZGMY37lzId43O94l72pMf9XaRR92veZcjjkdtF4w130_provenance.