Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP472209.RAB2W7cs9Lb7F0jt0QxF6E3t29YaL34VowGSR5ZZyZjZc130_assertion> ?p ?o ?g. }
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- NP472209.RAB2W7cs9Lb7F0jt0QxF6E3t29YaL34VowGSR5ZZyZjZc130_assertion type Assertion NP472209.RAB2W7cs9Lb7F0jt0QxF6E3t29YaL34VowGSR5ZZyZjZc130_head.
- NP472209.RAB2W7cs9Lb7F0jt0QxF6E3t29YaL34VowGSR5ZZyZjZc130_assertion description "[Defects in myosin VIIa, harmonin (a PDZ domain protein), cadherin 23, protocadherin 15 and sans (a putative scaffolding protein), underlie five forms of Usher syndrome type I (USH1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472209.RAB2W7cs9Lb7F0jt0QxF6E3t29YaL34VowGSR5ZZyZjZc130_provenance.
- NP472209.RAB2W7cs9Lb7F0jt0QxF6E3t29YaL34VowGSR5ZZyZjZc130_assertion evidence source_evidence_literature NP472209.RAB2W7cs9Lb7F0jt0QxF6E3t29YaL34VowGSR5ZZyZjZc130_provenance.
- NP472209.RAB2W7cs9Lb7F0jt0QxF6E3t29YaL34VowGSR5ZZyZjZc130_assertion SIO_000772 15590703 NP472209.RAB2W7cs9Lb7F0jt0QxF6E3t29YaL34VowGSR5ZZyZjZc130_provenance.
- NP472209.RAB2W7cs9Lb7F0jt0QxF6E3t29YaL34VowGSR5ZZyZjZc130_assertion wasDerivedFrom befree-2016 NP472209.RAB2W7cs9Lb7F0jt0QxF6E3t29YaL34VowGSR5ZZyZjZc130_provenance.
- NP472209.RAB2W7cs9Lb7F0jt0QxF6E3t29YaL34VowGSR5ZZyZjZc130_assertion wasGeneratedBy ECO_0000203 NP472209.RAB2W7cs9Lb7F0jt0QxF6E3t29YaL34VowGSR5ZZyZjZc130_provenance.