Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP773.RABqD1EHZeoT24J16qJQbFm_QAK6-4wm7UOG75uXlm9oo130_assertion> ?p ?o ?g. }
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- NP773.RABqD1EHZeoT24J16qJQbFm_QAK6-4wm7UOG75uXlm9oo130_assertion type Assertion NP773.RABqD1EHZeoT24J16qJQbFm_QAK6-4wm7UOG75uXlm9oo130_head.
- NP773.RABqD1EHZeoT24J16qJQbFm_QAK6-4wm7UOG75uXlm9oo130_assertion wasGeneratedBy ECO_0000218 NP773.RABqD1EHZeoT24J16qJQbFm_QAK6-4wm7UOG75uXlm9oo130_provenance.
- NP773.RABqD1EHZeoT24J16qJQbFm_QAK6-4wm7UOG75uXlm9oo130_assertion wasDerivedFrom uniprot-2016 NP773.RABqD1EHZeoT24J16qJQbFm_QAK6-4wm7UOG75uXlm9oo130_provenance.
- NP773.RABqD1EHZeoT24J16qJQbFm_QAK6-4wm7UOG75uXlm9oo130_assertion SIO_000772 10775529 NP773.RABqD1EHZeoT24J16qJQbFm_QAK6-4wm7UOG75uXlm9oo130_provenance.
- NP773.RABqD1EHZeoT24J16qJQbFm_QAK6-4wm7UOG75uXlm9oo130_assertion evidence source_evidence_curated NP773.RABqD1EHZeoT24J16qJQbFm_QAK6-4wm7UOG75uXlm9oo130_provenance.
- NP773.RABqD1EHZeoT24J16qJQbFm_QAK6-4wm7UOG75uXlm9oo130_assertion description "[Missense mutation in the USH2A gene: association with recessive retinitis pigmentosa without hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP773.RABqD1EHZeoT24J16qJQbFm_QAK6-4wm7UOG75uXlm9oo130_provenance.