Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_assertion> ?p ?o ?g. }
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- NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_assertion type Assertion NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_head.
- NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_assertion description "[This family represents a new syndrome (Mohr-Tranebjaerg syndrome, MTS) and provides significant new information about a new X linked recessive sydromic type of deafness which was previously thought to be isolated deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_provenance.
- NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_assertion evidence source_evidence_literature NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_provenance.
- NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_assertion SIO_000772 7643352 NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_provenance.
- NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_assertion wasDerivedFrom befree-20150227 NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_provenance.
- NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_assertion wasGeneratedBy ECO_0000203 NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_provenance.