Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP959588.RAXvWTlU7yGfsS1h6kjBvHiz_d1ZICNAnFoFnj3Q9uT0A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP959588.RAXvWTlU7yGfsS1h6kjBvHiz_d1ZICNAnFoFnj3Q9uT0A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP959588.RAXvWTlU7yGfsS1h6kjBvHiz_d1ZICNAnFoFnj3Q9uT0A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP959588.RAXvWTlU7yGfsS1h6kjBvHiz_d1ZICNAnFoFnj3Q9uT0A130_provenance.
- NP959588.RAXvWTlU7yGfsS1h6kjBvHiz_d1ZICNAnFoFnj3Q9uT0A130_assertion description "[A total of 103 patients with either CPHD (n = 35) or SOD (n = 68) were investigated for mutations in genes implicated in the etiology of KS (FGFR1, FGF8, PROKR2, PROK2, and KAL1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959588.RAXvWTlU7yGfsS1h6kjBvHiz_d1ZICNAnFoFnj3Q9uT0A130_provenance.
- NP959588.RAXvWTlU7yGfsS1h6kjBvHiz_d1ZICNAnFoFnj3Q9uT0A130_assertion evidence source_evidence_literature NP959588.RAXvWTlU7yGfsS1h6kjBvHiz_d1ZICNAnFoFnj3Q9uT0A130_provenance.
- NP959588.RAXvWTlU7yGfsS1h6kjBvHiz_d1ZICNAnFoFnj3Q9uT0A130_assertion SIO_000772 22319038 NP959588.RAXvWTlU7yGfsS1h6kjBvHiz_d1ZICNAnFoFnj3Q9uT0A130_provenance.
- NP959588.RAXvWTlU7yGfsS1h6kjBvHiz_d1ZICNAnFoFnj3Q9uT0A130_assertion wasDerivedFrom befree-2016 NP959588.RAXvWTlU7yGfsS1h6kjBvHiz_d1ZICNAnFoFnj3Q9uT0A130_provenance.
- NP959588.RAXvWTlU7yGfsS1h6kjBvHiz_d1ZICNAnFoFnj3Q9uT0A130_assertion wasGeneratedBy ECO_0000203 NP959588.RAXvWTlU7yGfsS1h6kjBvHiz_d1ZICNAnFoFnj3Q9uT0A130_provenance.
- befree-2016 importedOn "2016-02-19" NP959588.RAXvWTlU7yGfsS1h6kjBvHiz_d1ZICNAnFoFnj3Q9uT0A130_provenance.