Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP192737.RAq8TcZ5YeFZNWbeUhGISCQlyCMyTYG8tc5MQ9YqBearU130_assertion> ?p ?o ?g. }
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- NP192737.RAq8TcZ5YeFZNWbeUhGISCQlyCMyTYG8tc5MQ9YqBearU130_assertion type Assertion NP192737.RAq8TcZ5YeFZNWbeUhGISCQlyCMyTYG8tc5MQ9YqBearU130_head.
- NP192737.RAq8TcZ5YeFZNWbeUhGISCQlyCMyTYG8tc5MQ9YqBearU130_assertion description "[Suggested as a candidate gene for a dominant syndrome that consists of inclusion body myopathy, Paget disease of bone, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP192737.RAq8TcZ5YeFZNWbeUhGISCQlyCMyTYG8tc5MQ9YqBearU130_provenance.
- NP192737.RAq8TcZ5YeFZNWbeUhGISCQlyCMyTYG8tc5MQ9YqBearU130_assertion evidence source_evidence_literature NP192737.RAq8TcZ5YeFZNWbeUhGISCQlyCMyTYG8tc5MQ9YqBearU130_provenance.
- NP192737.RAq8TcZ5YeFZNWbeUhGISCQlyCMyTYG8tc5MQ9YqBearU130_assertion SIO_000772 11749051 NP192737.RAq8TcZ5YeFZNWbeUhGISCQlyCMyTYG8tc5MQ9YqBearU130_provenance.
- NP192737.RAq8TcZ5YeFZNWbeUhGISCQlyCMyTYG8tc5MQ9YqBearU130_assertion wasDerivedFrom lhgdn-20090331 NP192737.RAq8TcZ5YeFZNWbeUhGISCQlyCMyTYG8tc5MQ9YqBearU130_provenance.
- NP192737.RAq8TcZ5YeFZNWbeUhGISCQlyCMyTYG8tc5MQ9YqBearU130_assertion wasGeneratedBy ECO_0000203 NP192737.RAq8TcZ5YeFZNWbeUhGISCQlyCMyTYG8tc5MQ9YqBearU130_provenance.