Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP955421.RAATtw4jHSRkVo9XJ8d75AfNkD77-bZCvR4BTqGTbjmwU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP955421.RAATtw4jHSRkVo9XJ8d75AfNkD77-bZCvR4BTqGTbjmwU130_assertion type Assertion NP955421.RAATtw4jHSRkVo9XJ8d75AfNkD77-bZCvR4BTqGTbjmwU130_head.
- NP955421.RAATtw4jHSRkVo9XJ8d75AfNkD77-bZCvR4BTqGTbjmwU130_assertion wasGeneratedBy ECO_0000203 NP955421.RAATtw4jHSRkVo9XJ8d75AfNkD77-bZCvR4BTqGTbjmwU130_provenance.
- NP955421.RAATtw4jHSRkVo9XJ8d75AfNkD77-bZCvR4BTqGTbjmwU130_assertion wasDerivedFrom befree-20150227 NP955421.RAATtw4jHSRkVo9XJ8d75AfNkD77-bZCvR4BTqGTbjmwU130_provenance.
- NP955421.RAATtw4jHSRkVo9XJ8d75AfNkD77-bZCvR4BTqGTbjmwU130_assertion SIO_000772 20405026 NP955421.RAATtw4jHSRkVo9XJ8d75AfNkD77-bZCvR4BTqGTbjmwU130_provenance.
- NP955421.RAATtw4jHSRkVo9XJ8d75AfNkD77-bZCvR4BTqGTbjmwU130_assertion evidence source_evidence_literature NP955421.RAATtw4jHSRkVo9XJ8d75AfNkD77-bZCvR4BTqGTbjmwU130_provenance.
- NP955421.RAATtw4jHSRkVo9XJ8d75AfNkD77-bZCvR4BTqGTbjmwU130_assertion description "[Nonsense mutation in TMEM126A causing autosomal recessive optic atrophy and auditory neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP955421.RAATtw4jHSRkVo9XJ8d75AfNkD77-bZCvR4BTqGTbjmwU130_provenance.