Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP43054.RAGLvwGgL86aF2_WwLfrU8ncNoawBzUBZ2GpUMWTqM6qw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP43054.RAGLvwGgL86aF2_WwLfrU8ncNoawBzUBZ2GpUMWTqM6qw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP43054.RAGLvwGgL86aF2_WwLfrU8ncNoawBzUBZ2GpUMWTqM6qw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP43054.RAGLvwGgL86aF2_WwLfrU8ncNoawBzUBZ2GpUMWTqM6qw130_provenance.
- NP43054.RAGLvwGgL86aF2_WwLfrU8ncNoawBzUBZ2GpUMWTqM6qw130_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." NP43054.RAGLvwGgL86aF2_WwLfrU8ncNoawBzUBZ2GpUMWTqM6qw130_provenance.
- NP43054.RAGLvwGgL86aF2_WwLfrU8ncNoawBzUBZ2GpUMWTqM6qw130_assertion evidence source_evidence_literature NP43054.RAGLvwGgL86aF2_WwLfrU8ncNoawBzUBZ2GpUMWTqM6qw130_provenance.
- NP43054.RAGLvwGgL86aF2_WwLfrU8ncNoawBzUBZ2GpUMWTqM6qw130_assertion SIO_000772 15115915 NP43054.RAGLvwGgL86aF2_WwLfrU8ncNoawBzUBZ2GpUMWTqM6qw130_provenance.
- NP43054.RAGLvwGgL86aF2_WwLfrU8ncNoawBzUBZ2GpUMWTqM6qw130_assertion wasDerivedFrom gad-20130706 NP43054.RAGLvwGgL86aF2_WwLfrU8ncNoawBzUBZ2GpUMWTqM6qw130_provenance.
- NP43054.RAGLvwGgL86aF2_WwLfrU8ncNoawBzUBZ2GpUMWTqM6qw130_assertion wasGeneratedBy ECO_0000203 NP43054.RAGLvwGgL86aF2_WwLfrU8ncNoawBzUBZ2GpUMWTqM6qw130_provenance.
- gad-20130706 importedOn "2013-07-06" NP43054.RAGLvwGgL86aF2_WwLfrU8ncNoawBzUBZ2GpUMWTqM6qw130_provenance.