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- NP462403.RAtMsLf6qTjdqpH0goIP4PFfkiPwAuGdRFsoFKaySwPik130_assertion type Assertion NP462403.RAtMsLf6qTjdqpH0goIP4PFfkiPwAuGdRFsoFKaySwPik130_head.
- NP462403.RAtMsLf6qTjdqpH0goIP4PFfkiPwAuGdRFsoFKaySwPik130_assertion wasGeneratedBy ECO_0000203 NP462403.RAtMsLf6qTjdqpH0goIP4PFfkiPwAuGdRFsoFKaySwPik130_provenance.
- NP462403.RAtMsLf6qTjdqpH0goIP4PFfkiPwAuGdRFsoFKaySwPik130_assertion wasDerivedFrom befree-20140225 NP462403.RAtMsLf6qTjdqpH0goIP4PFfkiPwAuGdRFsoFKaySwPik130_provenance.
- NP462403.RAtMsLf6qTjdqpH0goIP4PFfkiPwAuGdRFsoFKaySwPik130_assertion SIO_000772 20642360 NP462403.RAtMsLf6qTjdqpH0goIP4PFfkiPwAuGdRFsoFKaySwPik130_provenance.
- NP462403.RAtMsLf6qTjdqpH0goIP4PFfkiPwAuGdRFsoFKaySwPik130_assertion evidence source_evidence_literature NP462403.RAtMsLf6qTjdqpH0goIP4PFfkiPwAuGdRFsoFKaySwPik130_provenance.
- NP462403.RAtMsLf6qTjdqpH0goIP4PFfkiPwAuGdRFsoFKaySwPik130_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." NP462403.RAtMsLf6qTjdqpH0goIP4PFfkiPwAuGdRFsoFKaySwPik130_provenance.