Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1238079.RA0CoJb0bS5Sst0KbHRNi-ewsuPqWjFti0idfLDS4JILQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1238079.RA0CoJb0bS5Sst0KbHRNi-ewsuPqWjFti0idfLDS4JILQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1238079.RA0CoJb0bS5Sst0KbHRNi-ewsuPqWjFti0idfLDS4JILQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1238079.RA0CoJb0bS5Sst0KbHRNi-ewsuPqWjFti0idfLDS4JILQ130_provenance.
- NP1238079.RA0CoJb0bS5Sst0KbHRNi-ewsuPqWjFti0idfLDS4JILQ130_assertion description "[A custom HaloPlex panel for Illumina platforms was designed to capture all exons of the 10 known causative Usher syndrome genes (MYO7A, USH1C, CDH23, PCDH15, USH1G, CIB2, USH2A, GPR98, DFNB31 and CLRN1), the two Usher syndrome-related genes (HARS and PDZD7) and the two candidate genes VEZT and MYO15A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1238079.RA0CoJb0bS5Sst0KbHRNi-ewsuPqWjFti0idfLDS4JILQ130_provenance.
- NP1238079.RA0CoJb0bS5Sst0KbHRNi-ewsuPqWjFti0idfLDS4JILQ130_assertion evidence source_evidence_literature NP1238079.RA0CoJb0bS5Sst0KbHRNi-ewsuPqWjFti0idfLDS4JILQ130_provenance.
- NP1238079.RA0CoJb0bS5Sst0KbHRNi-ewsuPqWjFti0idfLDS4JILQ130_assertion SIO_000772 25404053 NP1238079.RA0CoJb0bS5Sst0KbHRNi-ewsuPqWjFti0idfLDS4JILQ130_provenance.
- NP1238079.RA0CoJb0bS5Sst0KbHRNi-ewsuPqWjFti0idfLDS4JILQ130_assertion wasDerivedFrom befree-2016 NP1238079.RA0CoJb0bS5Sst0KbHRNi-ewsuPqWjFti0idfLDS4JILQ130_provenance.
- NP1238079.RA0CoJb0bS5Sst0KbHRNi-ewsuPqWjFti0idfLDS4JILQ130_assertion wasGeneratedBy ECO_0000203 NP1238079.RA0CoJb0bS5Sst0KbHRNi-ewsuPqWjFti0idfLDS4JILQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1238079.RA0CoJb0bS5Sst0KbHRNi-ewsuPqWjFti0idfLDS4JILQ130_provenance.