Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP198147.RATxSSHp9TQQ7GdsU2KR_M4D89XWG7RW794Ea6ISEQ7dk130_assertion> ?p ?o ?g. }
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- NP198147.RATxSSHp9TQQ7GdsU2KR_M4D89XWG7RW794Ea6ISEQ7dk130_assertion type Assertion NP198147.RATxSSHp9TQQ7GdsU2KR_M4D89XWG7RW794Ea6ISEQ7dk130_head.
- NP198147.RATxSSHp9TQQ7GdsU2KR_M4D89XWG7RW794Ea6ISEQ7dk130_assertion wasGeneratedBy ECO_0000203 NP198147.RATxSSHp9TQQ7GdsU2KR_M4D89XWG7RW794Ea6ISEQ7dk130_provenance.
- NP198147.RATxSSHp9TQQ7GdsU2KR_M4D89XWG7RW794Ea6ISEQ7dk130_assertion wasDerivedFrom lhgdn-20090331 NP198147.RATxSSHp9TQQ7GdsU2KR_M4D89XWG7RW794Ea6ISEQ7dk130_provenance.
- NP198147.RATxSSHp9TQQ7GdsU2KR_M4D89XWG7RW794Ea6ISEQ7dk130_assertion SIO_000772 17457594 NP198147.RATxSSHp9TQQ7GdsU2KR_M4D89XWG7RW794Ea6ISEQ7dk130_provenance.
- NP198147.RATxSSHp9TQQ7GdsU2KR_M4D89XWG7RW794Ea6ISEQ7dk130_assertion evidence source_evidence_literature NP198147.RATxSSHp9TQQ7GdsU2KR_M4D89XWG7RW794Ea6ISEQ7dk130_provenance.
- NP198147.RATxSSHp9TQQ7GdsU2KR_M4D89XWG7RW794Ea6ISEQ7dk130_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." NP198147.RATxSSHp9TQQ7GdsU2KR_M4D89XWG7RW794Ea6ISEQ7dk130_provenance.