Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP529531.RATmRjrCJjQbXRhOsK1o6ojMLAcGhXTWnvY_J1-4vmyL8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP529531.RATmRjrCJjQbXRhOsK1o6ojMLAcGhXTWnvY_J1-4vmyL8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP529531.RATmRjrCJjQbXRhOsK1o6ojMLAcGhXTWnvY_J1-4vmyL8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP529531.RATmRjrCJjQbXRhOsK1o6ojMLAcGhXTWnvY_J1-4vmyL8130_provenance.
- NP529531.RATmRjrCJjQbXRhOsK1o6ojMLAcGhXTWnvY_J1-4vmyL8130_assertion description "[Two novel disease-causing mutations in the CLRN1 gene in patients with Usher syndrome type 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP529531.RATmRjrCJjQbXRhOsK1o6ojMLAcGhXTWnvY_J1-4vmyL8130_provenance.
- NP529531.RATmRjrCJjQbXRhOsK1o6ojMLAcGhXTWnvY_J1-4vmyL8130_assertion evidence source_evidence_literature NP529531.RATmRjrCJjQbXRhOsK1o6ojMLAcGhXTWnvY_J1-4vmyL8130_provenance.
- NP529531.RATmRjrCJjQbXRhOsK1o6ojMLAcGhXTWnvY_J1-4vmyL8130_assertion SIO_000772 23304067 NP529531.RATmRjrCJjQbXRhOsK1o6ojMLAcGhXTWnvY_J1-4vmyL8130_provenance.
- NP529531.RATmRjrCJjQbXRhOsK1o6ojMLAcGhXTWnvY_J1-4vmyL8130_assertion wasDerivedFrom befree-20140225 NP529531.RATmRjrCJjQbXRhOsK1o6ojMLAcGhXTWnvY_J1-4vmyL8130_provenance.
- NP529531.RATmRjrCJjQbXRhOsK1o6ojMLAcGhXTWnvY_J1-4vmyL8130_assertion wasGeneratedBy ECO_0000203 NP529531.RATmRjrCJjQbXRhOsK1o6ojMLAcGhXTWnvY_J1-4vmyL8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP529531.RATmRjrCJjQbXRhOsK1o6ojMLAcGhXTWnvY_J1-4vmyL8130_provenance.