Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1003440.RAjyR37Tal4cl9A6YzDi4j3qnWvAD2ql47vbOBzQYg38o130_assertion> ?p ?o ?g. }
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- NP1003440.RAjyR37Tal4cl9A6YzDi4j3qnWvAD2ql47vbOBzQYg38o130_assertion type Assertion NP1003440.RAjyR37Tal4cl9A6YzDi4j3qnWvAD2ql47vbOBzQYg38o130_head.
- NP1003440.RAjyR37Tal4cl9A6YzDi4j3qnWvAD2ql47vbOBzQYg38o130_assertion description "[We and others have shown recently that mutations in the OPA1 gene encoding a dynamin-related mitochondrial protein cause autosomal dominant optic atrophy (ADOA) linked to chromosome 3q28-q29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1003440.RAjyR37Tal4cl9A6YzDi4j3qnWvAD2ql47vbOBzQYg38o130_provenance.
- NP1003440.RAjyR37Tal4cl9A6YzDi4j3qnWvAD2ql47vbOBzQYg38o130_assertion evidence source_evidence_literature NP1003440.RAjyR37Tal4cl9A6YzDi4j3qnWvAD2ql47vbOBzQYg38o130_provenance.
- NP1003440.RAjyR37Tal4cl9A6YzDi4j3qnWvAD2ql47vbOBzQYg38o130_assertion SIO_000772 11440988 NP1003440.RAjyR37Tal4cl9A6YzDi4j3qnWvAD2ql47vbOBzQYg38o130_provenance.
- NP1003440.RAjyR37Tal4cl9A6YzDi4j3qnWvAD2ql47vbOBzQYg38o130_assertion wasDerivedFrom befree-20150227 NP1003440.RAjyR37Tal4cl9A6YzDi4j3qnWvAD2ql47vbOBzQYg38o130_provenance.
- NP1003440.RAjyR37Tal4cl9A6YzDi4j3qnWvAD2ql47vbOBzQYg38o130_assertion wasGeneratedBy ECO_0000203 NP1003440.RAjyR37Tal4cl9A6YzDi4j3qnWvAD2ql47vbOBzQYg38o130_provenance.