Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP85267.RArTo5M_vED8FNyPY6kX49twalcFbCuFp8GAzbGHKumig130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP85267.RArTo5M_vED8FNyPY6kX49twalcFbCuFp8GAzbGHKumig130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP85267.RArTo5M_vED8FNyPY6kX49twalcFbCuFp8GAzbGHKumig130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP85267.RArTo5M_vED8FNyPY6kX49twalcFbCuFp8GAzbGHKumig130_provenance.
- NP85267.RArTo5M_vED8FNyPY6kX49twalcFbCuFp8GAzbGHKumig130_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." NP85267.RArTo5M_vED8FNyPY6kX49twalcFbCuFp8GAzbGHKumig130_provenance.
- NP85267.RArTo5M_vED8FNyPY6kX49twalcFbCuFp8GAzbGHKumig130_assertion evidence source_evidence_literature NP85267.RArTo5M_vED8FNyPY6kX49twalcFbCuFp8GAzbGHKumig130_provenance.
- NP85267.RArTo5M_vED8FNyPY6kX49twalcFbCuFp8GAzbGHKumig130_assertion SIO_000772 15115915 NP85267.RArTo5M_vED8FNyPY6kX49twalcFbCuFp8GAzbGHKumig130_provenance.
- NP85267.RArTo5M_vED8FNyPY6kX49twalcFbCuFp8GAzbGHKumig130_assertion wasDerivedFrom gad-20150221 NP85267.RArTo5M_vED8FNyPY6kX49twalcFbCuFp8GAzbGHKumig130_provenance.
- NP85267.RArTo5M_vED8FNyPY6kX49twalcFbCuFp8GAzbGHKumig130_assertion wasGeneratedBy ECO_0000203 NP85267.RArTo5M_vED8FNyPY6kX49twalcFbCuFp8GAzbGHKumig130_provenance.
- gad-20150221 importedOn "2015-02-21" NP85267.RArTo5M_vED8FNyPY6kX49twalcFbCuFp8GAzbGHKumig130_provenance.