Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP823258.RAoPX3kt2vcTv2EUyeLX2yhO67ZArQoGatAxOFiv-4V9c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP823258.RAoPX3kt2vcTv2EUyeLX2yhO67ZArQoGatAxOFiv-4V9c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP823258.RAoPX3kt2vcTv2EUyeLX2yhO67ZArQoGatAxOFiv-4V9c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP823258.RAoPX3kt2vcTv2EUyeLX2yhO67ZArQoGatAxOFiv-4V9c130_provenance.
- NP823258.RAoPX3kt2vcTv2EUyeLX2yhO67ZArQoGatAxOFiv-4V9c130_assertion description "[We tested 303 unrelated Czech patients with early hearing loss (298 with NSHL and 5 with PS), all GJB2-negative, for SLC26A4 mutations and evaluated their clinical and radiological phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP823258.RAoPX3kt2vcTv2EUyeLX2yhO67ZArQoGatAxOFiv-4V9c130_provenance.
- NP823258.RAoPX3kt2vcTv2EUyeLX2yhO67ZArQoGatAxOFiv-4V9c130_assertion evidence source_evidence_literature NP823258.RAoPX3kt2vcTv2EUyeLX2yhO67ZArQoGatAxOFiv-4V9c130_provenance.
- NP823258.RAoPX3kt2vcTv2EUyeLX2yhO67ZArQoGatAxOFiv-4V9c130_assertion SIO_000772 20597900 NP823258.RAoPX3kt2vcTv2EUyeLX2yhO67ZArQoGatAxOFiv-4V9c130_provenance.
- NP823258.RAoPX3kt2vcTv2EUyeLX2yhO67ZArQoGatAxOFiv-4V9c130_assertion wasDerivedFrom befree-2016 NP823258.RAoPX3kt2vcTv2EUyeLX2yhO67ZArQoGatAxOFiv-4V9c130_provenance.
- NP823258.RAoPX3kt2vcTv2EUyeLX2yhO67ZArQoGatAxOFiv-4V9c130_assertion wasGeneratedBy ECO_0000203 NP823258.RAoPX3kt2vcTv2EUyeLX2yhO67ZArQoGatAxOFiv-4V9c130_provenance.
- befree-2016 importedOn "2016-02-19" NP823258.RAoPX3kt2vcTv2EUyeLX2yhO67ZArQoGatAxOFiv-4V9c130_provenance.