Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1249634.RAQJw6w67dyThgAFMVJJecM2YQc3v6awvz2EoCROceZgg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1249634.RAQJw6w67dyThgAFMVJJecM2YQc3v6awvz2EoCROceZgg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1249634.RAQJw6w67dyThgAFMVJJecM2YQc3v6awvz2EoCROceZgg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1249634.RAQJw6w67dyThgAFMVJJecM2YQc3v6awvz2EoCROceZgg130_provenance.
- NP1249634.RAQJw6w67dyThgAFMVJJecM2YQc3v6awvz2EoCROceZgg130_assertion description "[Detection of mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 families with early-onset high myopia by exome sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249634.RAQJw6w67dyThgAFMVJJecM2YQc3v6awvz2EoCROceZgg130_provenance.
- NP1249634.RAQJw6w67dyThgAFMVJJecM2YQc3v6awvz2EoCROceZgg130_assertion evidence source_evidence_literature NP1249634.RAQJw6w67dyThgAFMVJJecM2YQc3v6awvz2EoCROceZgg130_provenance.
- NP1249634.RAQJw6w67dyThgAFMVJJecM2YQc3v6awvz2EoCROceZgg130_assertion SIO_000772 25525168 NP1249634.RAQJw6w67dyThgAFMVJJecM2YQc3v6awvz2EoCROceZgg130_provenance.
- NP1249634.RAQJw6w67dyThgAFMVJJecM2YQc3v6awvz2EoCROceZgg130_assertion wasDerivedFrom befree-2016 NP1249634.RAQJw6w67dyThgAFMVJJecM2YQc3v6awvz2EoCROceZgg130_provenance.
- NP1249634.RAQJw6w67dyThgAFMVJJecM2YQc3v6awvz2EoCROceZgg130_assertion wasGeneratedBy ECO_0000203 NP1249634.RAQJw6w67dyThgAFMVJJecM2YQc3v6awvz2EoCROceZgg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1249634.RAQJw6w67dyThgAFMVJJecM2YQc3v6awvz2EoCROceZgg130_provenance.