Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP398245.RAGnlXQeYV89Diim2eE5Ym96iuiyTy0CFXTW58Eo3imKY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP398245.RAGnlXQeYV89Diim2eE5Ym96iuiyTy0CFXTW58Eo3imKY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP398245.RAGnlXQeYV89Diim2eE5Ym96iuiyTy0CFXTW58Eo3imKY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP398245.RAGnlXQeYV89Diim2eE5Ym96iuiyTy0CFXTW58Eo3imKY130_provenance.
- NP398245.RAGnlXQeYV89Diim2eE5Ym96iuiyTy0CFXTW58Eo3imKY130_assertion description "[Co-occurring PTPN11 and SOS1 gene mutations in Noonan syndrome: does this predict a more severe phenotype?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP398245.RAGnlXQeYV89Diim2eE5Ym96iuiyTy0CFXTW58Eo3imKY130_provenance.
- NP398245.RAGnlXQeYV89Diim2eE5Ym96iuiyTy0CFXTW58Eo3imKY130_assertion evidence source_evidence_literature NP398245.RAGnlXQeYV89Diim2eE5Ym96iuiyTy0CFXTW58Eo3imKY130_provenance.
- NP398245.RAGnlXQeYV89Diim2eE5Ym96iuiyTy0CFXTW58Eo3imKY130_assertion SIO_000772 21340158 NP398245.RAGnlXQeYV89Diim2eE5Ym96iuiyTy0CFXTW58Eo3imKY130_provenance.
- NP398245.RAGnlXQeYV89Diim2eE5Ym96iuiyTy0CFXTW58Eo3imKY130_assertion wasDerivedFrom befree-20140225 NP398245.RAGnlXQeYV89Diim2eE5Ym96iuiyTy0CFXTW58Eo3imKY130_provenance.
- NP398245.RAGnlXQeYV89Diim2eE5Ym96iuiyTy0CFXTW58Eo3imKY130_assertion wasGeneratedBy ECO_0000203 NP398245.RAGnlXQeYV89Diim2eE5Ym96iuiyTy0CFXTW58Eo3imKY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP398245.RAGnlXQeYV89Diim2eE5Ym96iuiyTy0CFXTW58Eo3imKY130_provenance.