Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP492018.RAgj2A9RDZgyA4MYd8pjLA-rup-KYaeEPXx4IJa2Leyw0130_assertion> ?p ?o ?g. }
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- NP492018.RAgj2A9RDZgyA4MYd8pjLA-rup-KYaeEPXx4IJa2Leyw0130_assertion type Assertion NP492018.RAgj2A9RDZgyA4MYd8pjLA-rup-KYaeEPXx4IJa2Leyw0130_head.
- NP492018.RAgj2A9RDZgyA4MYd8pjLA-rup-KYaeEPXx4IJa2Leyw0130_assertion wasGeneratedBy ECO_0000203 NP492018.RAgj2A9RDZgyA4MYd8pjLA-rup-KYaeEPXx4IJa2Leyw0130_provenance.
- NP492018.RAgj2A9RDZgyA4MYd8pjLA-rup-KYaeEPXx4IJa2Leyw0130_assertion wasDerivedFrom befree-20140225 NP492018.RAgj2A9RDZgyA4MYd8pjLA-rup-KYaeEPXx4IJa2Leyw0130_provenance.
- NP492018.RAgj2A9RDZgyA4MYd8pjLA-rup-KYaeEPXx4IJa2Leyw0130_assertion SIO_000772 16459341 NP492018.RAgj2A9RDZgyA4MYd8pjLA-rup-KYaeEPXx4IJa2Leyw0130_provenance.
- NP492018.RAgj2A9RDZgyA4MYd8pjLA-rup-KYaeEPXx4IJa2Leyw0130_assertion evidence source_evidence_literature NP492018.RAgj2A9RDZgyA4MYd8pjLA-rup-KYaeEPXx4IJa2Leyw0130_provenance.
- NP492018.RAgj2A9RDZgyA4MYd8pjLA-rup-KYaeEPXx4IJa2Leyw0130_assertion description "[Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492018.RAgj2A9RDZgyA4MYd8pjLA-rup-KYaeEPXx4IJa2Leyw0130_provenance.