Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3898.RAHIQ1wvI8jpHQa1rddIp455kkJICGYvJ79NqckSZeWrw130_assertion> ?p ?o ?g. }
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- NP3898.RAHIQ1wvI8jpHQa1rddIp455kkJICGYvJ79NqckSZeWrw130_assertion type Assertion NP3898.RAHIQ1wvI8jpHQa1rddIp455kkJICGYvJ79NqckSZeWrw130_head.
- NP3898.RAHIQ1wvI8jpHQa1rddIp455kkJICGYvJ79NqckSZeWrw130_assertion description "[We report here that mutations of LRTOMT are associated with profound nonsyndromic hearing loss at the DFNB63 locus on human chromosome 11q13.3-q13.4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3898.RAHIQ1wvI8jpHQa1rddIp455kkJICGYvJ79NqckSZeWrw130_provenance.
- NP3898.RAHIQ1wvI8jpHQa1rddIp455kkJICGYvJ79NqckSZeWrw130_assertion evidence source_evidence_curated NP3898.RAHIQ1wvI8jpHQa1rddIp455kkJICGYvJ79NqckSZeWrw130_provenance.
- NP3898.RAHIQ1wvI8jpHQa1rddIp455kkJICGYvJ79NqckSZeWrw130_assertion SIO_000772 18953341 NP3898.RAHIQ1wvI8jpHQa1rddIp455kkJICGYvJ79NqckSZeWrw130_provenance.
- NP3898.RAHIQ1wvI8jpHQa1rddIp455kkJICGYvJ79NqckSZeWrw130_assertion wasDerivedFrom uniprot-20130724 NP3898.RAHIQ1wvI8jpHQa1rddIp455kkJICGYvJ79NqckSZeWrw130_provenance.
- NP3898.RAHIQ1wvI8jpHQa1rddIp455kkJICGYvJ79NqckSZeWrw130_assertion wasGeneratedBy ECO_0000218 NP3898.RAHIQ1wvI8jpHQa1rddIp455kkJICGYvJ79NqckSZeWrw130_provenance.