Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_provenance.
- 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.
- uniprot-2016 importedOn "2016-01-25" NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_provenance.