Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1176758.RAnEOXvrLB2fnRuxLXcMW1b3iwUDZGJe7SgmIsCc57qHE130_assertion> ?p ?o ?g. }
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- NP1176758.RAnEOXvrLB2fnRuxLXcMW1b3iwUDZGJe7SgmIsCc57qHE130_assertion type Assertion NP1176758.RAnEOXvrLB2fnRuxLXcMW1b3iwUDZGJe7SgmIsCc57qHE130_head.
- NP1176758.RAnEOXvrLB2fnRuxLXcMW1b3iwUDZGJe7SgmIsCc57qHE130_assertion description "[Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1176758.RAnEOXvrLB2fnRuxLXcMW1b3iwUDZGJe7SgmIsCc57qHE130_provenance.
- NP1176758.RAnEOXvrLB2fnRuxLXcMW1b3iwUDZGJe7SgmIsCc57qHE130_assertion evidence source_evidence_literature NP1176758.RAnEOXvrLB2fnRuxLXcMW1b3iwUDZGJe7SgmIsCc57qHE130_provenance.
- NP1176758.RAnEOXvrLB2fnRuxLXcMW1b3iwUDZGJe7SgmIsCc57qHE130_assertion SIO_000772 24767429 NP1176758.RAnEOXvrLB2fnRuxLXcMW1b3iwUDZGJe7SgmIsCc57qHE130_provenance.
- NP1176758.RAnEOXvrLB2fnRuxLXcMW1b3iwUDZGJe7SgmIsCc57qHE130_assertion wasDerivedFrom befree-2016 NP1176758.RAnEOXvrLB2fnRuxLXcMW1b3iwUDZGJe7SgmIsCc57qHE130_provenance.
- NP1176758.RAnEOXvrLB2fnRuxLXcMW1b3iwUDZGJe7SgmIsCc57qHE130_assertion wasGeneratedBy ECO_0000203 NP1176758.RAnEOXvrLB2fnRuxLXcMW1b3iwUDZGJe7SgmIsCc57qHE130_provenance.