Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP67906.RAmy5I1AYjVlapaRjEGXb_W6-sPCOnaslrzPScWlSgyzc130_assertion> ?p ?o ?g. }
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- NP67906.RAmy5I1AYjVlapaRjEGXb_W6-sPCOnaslrzPScWlSgyzc130_assertion type Assertion NP67906.RAmy5I1AYjVlapaRjEGXb_W6-sPCOnaslrzPScWlSgyzc130_head.
- NP67906.RAmy5I1AYjVlapaRjEGXb_W6-sPCOnaslrzPScWlSgyzc130_assertion description "[These results suggest that the different types of Cx26 mutations affect autosomal recessive NSHL according to ethnic background.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP67906.RAmy5I1AYjVlapaRjEGXb_W6-sPCOnaslrzPScWlSgyzc130_provenance.
- NP67906.RAmy5I1AYjVlapaRjEGXb_W6-sPCOnaslrzPScWlSgyzc130_assertion evidence source_evidence_literature NP67906.RAmy5I1AYjVlapaRjEGXb_W6-sPCOnaslrzPScWlSgyzc130_provenance.
- NP67906.RAmy5I1AYjVlapaRjEGXb_W6-sPCOnaslrzPScWlSgyzc130_assertion SIO_000772 10983956 NP67906.RAmy5I1AYjVlapaRjEGXb_W6-sPCOnaslrzPScWlSgyzc130_provenance.
- NP67906.RAmy5I1AYjVlapaRjEGXb_W6-sPCOnaslrzPScWlSgyzc130_assertion wasDerivedFrom gad-20150221 NP67906.RAmy5I1AYjVlapaRjEGXb_W6-sPCOnaslrzPScWlSgyzc130_provenance.
- NP67906.RAmy5I1AYjVlapaRjEGXb_W6-sPCOnaslrzPScWlSgyzc130_assertion wasGeneratedBy ECO_0000203 NP67906.RAmy5I1AYjVlapaRjEGXb_W6-sPCOnaslrzPScWlSgyzc130_provenance.