Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_assertion type Assertion NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_head.
- NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_assertion description "[Mutations in the human transmembrane protein CRB1 are associated with severe forms of retinal dystrophy, retinitis pigmentosa 12 (RP12), and Leber's congenital amaurosis (LCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_provenance.
- NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_assertion evidence source_evidence_literature NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_provenance.
- NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_assertion SIO_000772 12361571 NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_provenance.
- NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_assertion wasDerivedFrom befree-20140225 NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_provenance.
- NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_assertion wasGeneratedBy ECO_0000203 NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_provenance.