Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP990456.RAUCejTGri2WS__ZiR5WU4z9E1vTadORt5HRHNDQSOGVw130_assertion> ?p ?o ?g. }
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- NP990456.RAUCejTGri2WS__ZiR5WU4z9E1vTadORt5HRHNDQSOGVw130_assertion type Assertion NP990456.RAUCejTGri2WS__ZiR5WU4z9E1vTadORt5HRHNDQSOGVw130_head.
- NP990456.RAUCejTGri2WS__ZiR5WU4z9E1vTadORt5HRHNDQSOGVw130_assertion description "[Hearing loss in patients with GRXCR1 mutations is congenital and is moderate to profound.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990456.RAUCejTGri2WS__ZiR5WU4z9E1vTadORt5HRHNDQSOGVw130_provenance.
- NP990456.RAUCejTGri2WS__ZiR5WU4z9E1vTadORt5HRHNDQSOGVw130_assertion evidence source_evidence_literature NP990456.RAUCejTGri2WS__ZiR5WU4z9E1vTadORt5HRHNDQSOGVw130_provenance.
- NP990456.RAUCejTGri2WS__ZiR5WU4z9E1vTadORt5HRHNDQSOGVw130_assertion SIO_000772 20137778 NP990456.RAUCejTGri2WS__ZiR5WU4z9E1vTadORt5HRHNDQSOGVw130_provenance.
- NP990456.RAUCejTGri2WS__ZiR5WU4z9E1vTadORt5HRHNDQSOGVw130_assertion wasDerivedFrom befree-20150227 NP990456.RAUCejTGri2WS__ZiR5WU4z9E1vTadORt5HRHNDQSOGVw130_provenance.
- NP990456.RAUCejTGri2WS__ZiR5WU4z9E1vTadORt5HRHNDQSOGVw130_assertion wasGeneratedBy ECO_0000203 NP990456.RAUCejTGri2WS__ZiR5WU4z9E1vTadORt5HRHNDQSOGVw130_provenance.