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- NP902748.RAWfycDVHcPDQg03fZvwergnJBBkYUC04orb3hH1P2YbU130_assertion type Assertion NP902748.RAWfycDVHcPDQg03fZvwergnJBBkYUC04orb3hH1P2YbU130_head.
- NP902748.RAWfycDVHcPDQg03fZvwergnJBBkYUC04orb3hH1P2YbU130_assertion wasGeneratedBy ECO_0000203 NP902748.RAWfycDVHcPDQg03fZvwergnJBBkYUC04orb3hH1P2YbU130_provenance.
- NP902748.RAWfycDVHcPDQg03fZvwergnJBBkYUC04orb3hH1P2YbU130_assertion wasDerivedFrom befree-20150227 NP902748.RAWfycDVHcPDQg03fZvwergnJBBkYUC04orb3hH1P2YbU130_provenance.
- NP902748.RAWfycDVHcPDQg03fZvwergnJBBkYUC04orb3hH1P2YbU130_assertion SIO_000772 20642360 NP902748.RAWfycDVHcPDQg03fZvwergnJBBkYUC04orb3hH1P2YbU130_provenance.
- NP902748.RAWfycDVHcPDQg03fZvwergnJBBkYUC04orb3hH1P2YbU130_assertion evidence source_evidence_literature NP902748.RAWfycDVHcPDQg03fZvwergnJBBkYUC04orb3hH1P2YbU130_provenance.
- NP902748.RAWfycDVHcPDQg03fZvwergnJBBkYUC04orb3hH1P2YbU130_assertion description "[We screened the MYO15A gene for mutations in 104 unrelated multiplex and consanguineous Turkish families with autosomal recessive nonsyndromic sensorineural hearing loss using autozygosity mapping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP902748.RAWfycDVHcPDQg03fZvwergnJBBkYUC04orb3hH1P2YbU130_provenance.