Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1316313.RAsU3mqHRoKxyV7SQH4M6FGI5kUL_7XKp3hbiOF-n5r2U130_assertion> ?p ?o ?g. }
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- NP1316313.RAsU3mqHRoKxyV7SQH4M6FGI5kUL_7XKp3hbiOF-n5r2U130_assertion type Assertion NP1316313.RAsU3mqHRoKxyV7SQH4M6FGI5kUL_7XKp3hbiOF-n5r2U130_head.
- NP1316313.RAsU3mqHRoKxyV7SQH4M6FGI5kUL_7XKp3hbiOF-n5r2U130_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." NP1316313.RAsU3mqHRoKxyV7SQH4M6FGI5kUL_7XKp3hbiOF-n5r2U130_provenance.
- NP1316313.RAsU3mqHRoKxyV7SQH4M6FGI5kUL_7XKp3hbiOF-n5r2U130_assertion evidence source_evidence_literature NP1316313.RAsU3mqHRoKxyV7SQH4M6FGI5kUL_7XKp3hbiOF-n5r2U130_provenance.
- NP1316313.RAsU3mqHRoKxyV7SQH4M6FGI5kUL_7XKp3hbiOF-n5r2U130_assertion SIO_000772 7643352 NP1316313.RAsU3mqHRoKxyV7SQH4M6FGI5kUL_7XKp3hbiOF-n5r2U130_provenance.
- NP1316313.RAsU3mqHRoKxyV7SQH4M6FGI5kUL_7XKp3hbiOF-n5r2U130_assertion wasDerivedFrom befree-2016 NP1316313.RAsU3mqHRoKxyV7SQH4M6FGI5kUL_7XKp3hbiOF-n5r2U130_provenance.
- NP1316313.RAsU3mqHRoKxyV7SQH4M6FGI5kUL_7XKp3hbiOF-n5r2U130_assertion wasGeneratedBy ECO_0000203 NP1316313.RAsU3mqHRoKxyV7SQH4M6FGI5kUL_7XKp3hbiOF-n5r2U130_provenance.