Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP1426.RAIOOFGLDXbqEJTw1-AOHVRHPs6jQBe7ix2G7uqtCX5a4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1426.RAIOOFGLDXbqEJTw1-AOHVRHPs6jQBe7ix2G7uqtCX5a4130_assertion type Assertion NP1426.RAIOOFGLDXbqEJTw1-AOHVRHPs6jQBe7ix2G7uqtCX5a4130_head.
- NP1426.RAIOOFGLDXbqEJTw1-AOHVRHPs6jQBe7ix2G7uqtCX5a4130_assertion wasGeneratedBy ECO_0000218 NP1426.RAIOOFGLDXbqEJTw1-AOHVRHPs6jQBe7ix2G7uqtCX5a4130_provenance.
- NP1426.RAIOOFGLDXbqEJTw1-AOHVRHPs6jQBe7ix2G7uqtCX5a4130_assertion wasDerivedFrom uniprot-20130724 NP1426.RAIOOFGLDXbqEJTw1-AOHVRHPs6jQBe7ix2G7uqtCX5a4130_provenance.
- NP1426.RAIOOFGLDXbqEJTw1-AOHVRHPs6jQBe7ix2G7uqtCX5a4130_assertion SIO_000772 15563506 NP1426.RAIOOFGLDXbqEJTw1-AOHVRHPs6jQBe7ix2G7uqtCX5a4130_provenance.
- NP1426.RAIOOFGLDXbqEJTw1-AOHVRHPs6jQBe7ix2G7uqtCX5a4130_assertion evidence source_evidence_curated NP1426.RAIOOFGLDXbqEJTw1-AOHVRHPs6jQBe7ix2G7uqtCX5a4130_provenance.
- NP1426.RAIOOFGLDXbqEJTw1-AOHVRHPs6jQBe7ix2G7uqtCX5a4130_assertion description "[Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1426.RAIOOFGLDXbqEJTw1-AOHVRHPs6jQBe7ix2G7uqtCX5a4130_provenance.