Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1598.RATYyvBnAN3ffbs6AkcAtenw_bqdtDQK2euS7mV0tYSPU130_assertion> ?p ?o ?g. }
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- NP1598.RATYyvBnAN3ffbs6AkcAtenw_bqdtDQK2euS7mV0tYSPU130_assertion type Assertion NP1598.RATYyvBnAN3ffbs6AkcAtenw_bqdtDQK2euS7mV0tYSPU130_head.
- NP1598.RATYyvBnAN3ffbs6AkcAtenw_bqdtDQK2euS7mV0tYSPU130_assertion wasGeneratedBy ECO_0000218 NP1598.RATYyvBnAN3ffbs6AkcAtenw_bqdtDQK2euS7mV0tYSPU130_provenance.
- NP1598.RATYyvBnAN3ffbs6AkcAtenw_bqdtDQK2euS7mV0tYSPU130_assertion wasDerivedFrom uniprot-2016 NP1598.RATYyvBnAN3ffbs6AkcAtenw_bqdtDQK2euS7mV0tYSPU130_provenance.
- NP1598.RATYyvBnAN3ffbs6AkcAtenw_bqdtDQK2euS7mV0tYSPU130_assertion SIO_000772 11524702 NP1598.RATYyvBnAN3ffbs6AkcAtenw_bqdtDQK2euS7mV0tYSPU130_provenance.
- NP1598.RATYyvBnAN3ffbs6AkcAtenw_bqdtDQK2euS7mV0tYSPU130_assertion evidence source_evidence_curated NP1598.RATYyvBnAN3ffbs6AkcAtenw_bqdtDQK2euS7mV0tYSPU130_provenance.
- NP1598.RATYyvBnAN3ffbs6AkcAtenw_bqdtDQK2euS7mV0tYSPU130_assertion description "[Usher syndrome type 3 (USH3) is an autosomal recessive disorder characterized by progressive hearing loss, severe retinal degeneration, and variably present vestibular dysfunction, assigned to 3q21-q25.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1598.RATYyvBnAN3ffbs6AkcAtenw_bqdtDQK2euS7mV0tYSPU130_provenance.