Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP866823.RAW2nNIPM_dmVhGU9-CcYTQR7GM4XfOhLGuXeJhweQqlQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP866823.RAW2nNIPM_dmVhGU9-CcYTQR7GM4XfOhLGuXeJhweQqlQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP866823.RAW2nNIPM_dmVhGU9-CcYTQR7GM4XfOhLGuXeJhweQqlQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP866823.RAW2nNIPM_dmVhGU9-CcYTQR7GM4XfOhLGuXeJhweQqlQ130_provenance.
- NP866823.RAW2nNIPM_dmVhGU9-CcYTQR7GM4XfOhLGuXeJhweQqlQ130_assertion description "[GPR98 mutations cause Usher syndrome type 2 in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866823.RAW2nNIPM_dmVhGU9-CcYTQR7GM4XfOhLGuXeJhweQqlQ130_provenance.
- NP866823.RAW2nNIPM_dmVhGU9-CcYTQR7GM4XfOhLGuXeJhweQqlQ130_assertion evidence source_evidence_literature NP866823.RAW2nNIPM_dmVhGU9-CcYTQR7GM4XfOhLGuXeJhweQqlQ130_provenance.
- NP866823.RAW2nNIPM_dmVhGU9-CcYTQR7GM4XfOhLGuXeJhweQqlQ130_assertion SIO_000772 19357117 NP866823.RAW2nNIPM_dmVhGU9-CcYTQR7GM4XfOhLGuXeJhweQqlQ130_provenance.
- NP866823.RAW2nNIPM_dmVhGU9-CcYTQR7GM4XfOhLGuXeJhweQqlQ130_assertion wasDerivedFrom befree-20140225 NP866823.RAW2nNIPM_dmVhGU9-CcYTQR7GM4XfOhLGuXeJhweQqlQ130_provenance.
- NP866823.RAW2nNIPM_dmVhGU9-CcYTQR7GM4XfOhLGuXeJhweQqlQ130_assertion wasGeneratedBy ECO_0000203 NP866823.RAW2nNIPM_dmVhGU9-CcYTQR7GM4XfOhLGuXeJhweQqlQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP866823.RAW2nNIPM_dmVhGU9-CcYTQR7GM4XfOhLGuXeJhweQqlQ130_provenance.