Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP50695.RAFJhKpPJY00WUzmGHH3YALqq6dM2CfgQiY51gaF-j7Rc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP50695.RAFJhKpPJY00WUzmGHH3YALqq6dM2CfgQiY51gaF-j7Rc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP50695.RAFJhKpPJY00WUzmGHH3YALqq6dM2CfgQiY51gaF-j7Rc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP50695.RAFJhKpPJY00WUzmGHH3YALqq6dM2CfgQiY51gaF-j7Rc130_provenance.
- NP50695.RAFJhKpPJY00WUzmGHH3YALqq6dM2CfgQiY51gaF-j7Rc130_assertion description "[ These data provide the first evidence suggesting that polymorphism of the GSTM3 gene contributes to clinical severity in CF, which may have prognostic significance and could prompt to start a more targeted therapy in young patients with CF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50695.RAFJhKpPJY00WUzmGHH3YALqq6dM2CfgQiY51gaF-j7Rc130_provenance.
- NP50695.RAFJhKpPJY00WUzmGHH3YALqq6dM2CfgQiY51gaF-j7Rc130_assertion evidence source_evidence_literature NP50695.RAFJhKpPJY00WUzmGHH3YALqq6dM2CfgQiY51gaF-j7Rc130_provenance.
- NP50695.RAFJhKpPJY00WUzmGHH3YALqq6dM2CfgQiY51gaF-j7Rc130_assertion SIO_000772 15115915 NP50695.RAFJhKpPJY00WUzmGHH3YALqq6dM2CfgQiY51gaF-j7Rc130_provenance.
- NP50695.RAFJhKpPJY00WUzmGHH3YALqq6dM2CfgQiY51gaF-j7Rc130_assertion wasDerivedFrom gad-20150221 NP50695.RAFJhKpPJY00WUzmGHH3YALqq6dM2CfgQiY51gaF-j7Rc130_provenance.
- NP50695.RAFJhKpPJY00WUzmGHH3YALqq6dM2CfgQiY51gaF-j7Rc130_assertion wasGeneratedBy ECO_0000203 NP50695.RAFJhKpPJY00WUzmGHH3YALqq6dM2CfgQiY51gaF-j7Rc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP50695.RAFJhKpPJY00WUzmGHH3YALqq6dM2CfgQiY51gaF-j7Rc130_provenance.