Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_assertion type Assertion NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_head.
- NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_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." NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_provenance.
- NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_assertion evidence source_evidence_curated NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_provenance.
- NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_assertion SIO_000772 18953341 NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_provenance.
- NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_assertion wasDerivedFrom uniprot-2016 NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_provenance.
- NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_assertion wasGeneratedBy ECO_0000218 NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_provenance.