Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP482536.RAm8VD4wPQO4gAJhOuM8ROYNIN8W1qLiEa8I6oUJmU8ZA130_assertion> ?p ?o ?g. }
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- NP482536.RAm8VD4wPQO4gAJhOuM8ROYNIN8W1qLiEa8I6oUJmU8ZA130_assertion type Assertion NP482536.RAm8VD4wPQO4gAJhOuM8ROYNIN8W1qLiEa8I6oUJmU8ZA130_head.
- NP482536.RAm8VD4wPQO4gAJhOuM8ROYNIN8W1qLiEa8I6oUJmU8ZA130_assertion description "[Mutations in the valosin-containing protein (VCP) gene on chromosome 9p13-p12 recently have been shown to cause autosomal dominant inclusion body myopathy associated with Paget's disease of the bone and frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP482536.RAm8VD4wPQO4gAJhOuM8ROYNIN8W1qLiEa8I6oUJmU8ZA130_provenance.
- NP482536.RAm8VD4wPQO4gAJhOuM8ROYNIN8W1qLiEa8I6oUJmU8ZA130_assertion evidence source_evidence_literature NP482536.RAm8VD4wPQO4gAJhOuM8ROYNIN8W1qLiEa8I6oUJmU8ZA130_provenance.
- NP482536.RAm8VD4wPQO4gAJhOuM8ROYNIN8W1qLiEa8I6oUJmU8ZA130_assertion SIO_000772 15732117 NP482536.RAm8VD4wPQO4gAJhOuM8ROYNIN8W1qLiEa8I6oUJmU8ZA130_provenance.
- NP482536.RAm8VD4wPQO4gAJhOuM8ROYNIN8W1qLiEa8I6oUJmU8ZA130_assertion wasDerivedFrom befree-2016 NP482536.RAm8VD4wPQO4gAJhOuM8ROYNIN8W1qLiEa8I6oUJmU8ZA130_provenance.
- NP482536.RAm8VD4wPQO4gAJhOuM8ROYNIN8W1qLiEa8I6oUJmU8ZA130_assertion wasGeneratedBy ECO_0000203 NP482536.RAm8VD4wPQO4gAJhOuM8ROYNIN8W1qLiEa8I6oUJmU8ZA130_provenance.