Matches in Nanopublications for { ?s ?p "[Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP314382.RA3maIwiCxZmYrK8WwSehBdIYIN41lMcUeWgThSe7atXk130_assertion description "[Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314382.RA3maIwiCxZmYrK8WwSehBdIYIN41lMcUeWgThSe7atXk130_provenance.
- NP980440.RAZ5XhwMjqo3-Ijur-21BspwLCZrcatn3oV1SSe0txV1M130_assertion description "[Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP980440.RAZ5XhwMjqo3-Ijur-21BspwLCZrcatn3oV1SSe0txV1M130_provenance.
- assertion description "[Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP700029.RAvWVvSk2WLOSE-jVW_xRHkqN_NVMq_5dF-0RcFGIzDIg130_assertion description "[Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP700029.RAvWVvSk2WLOSE-jVW_xRHkqN_NVMq_5dF-0RcFGIzDIg130_provenance.