Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP635837.RAlbRXMsiCMfNbN3ZR5D24CevFqGco8_hSn9Y_ps4OC1U130_assertion> ?p ?o ?g. }
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- NP635837.RAlbRXMsiCMfNbN3ZR5D24CevFqGco8_hSn9Y_ps4OC1U130_assertion type Assertion NP635837.RAlbRXMsiCMfNbN3ZR5D24CevFqGco8_hSn9Y_ps4OC1U130_head.
- NP635837.RAlbRXMsiCMfNbN3ZR5D24CevFqGco8_hSn9Y_ps4OC1U130_assertion description "[SNP linkage analysis and whole exome sequencing identify a novel POU4F3 mutation in autosomal dominant late-onset nonsyndromic hearing loss (DFNA15).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635837.RAlbRXMsiCMfNbN3ZR5D24CevFqGco8_hSn9Y_ps4OC1U130_provenance.
- NP635837.RAlbRXMsiCMfNbN3ZR5D24CevFqGco8_hSn9Y_ps4OC1U130_assertion evidence source_evidence_literature NP635837.RAlbRXMsiCMfNbN3ZR5D24CevFqGco8_hSn9Y_ps4OC1U130_provenance.
- NP635837.RAlbRXMsiCMfNbN3ZR5D24CevFqGco8_hSn9Y_ps4OC1U130_assertion SIO_000772 24260153 NP635837.RAlbRXMsiCMfNbN3ZR5D24CevFqGco8_hSn9Y_ps4OC1U130_provenance.
- NP635837.RAlbRXMsiCMfNbN3ZR5D24CevFqGco8_hSn9Y_ps4OC1U130_assertion wasDerivedFrom befree-20150227 NP635837.RAlbRXMsiCMfNbN3ZR5D24CevFqGco8_hSn9Y_ps4OC1U130_provenance.
- NP635837.RAlbRXMsiCMfNbN3ZR5D24CevFqGco8_hSn9Y_ps4OC1U130_assertion wasGeneratedBy ECO_0000203 NP635837.RAlbRXMsiCMfNbN3ZR5D24CevFqGco8_hSn9Y_ps4OC1U130_provenance.