Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP206907.RAIUfqtycepL2TIqxB73NJFpjQ3QAveCuqItsFV41Ys4s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP206907.RAIUfqtycepL2TIqxB73NJFpjQ3QAveCuqItsFV41Ys4s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP206907.RAIUfqtycepL2TIqxB73NJFpjQ3QAveCuqItsFV41Ys4s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP206907.RAIUfqtycepL2TIqxB73NJFpjQ3QAveCuqItsFV41Ys4s130_provenance.
- NP206907.RAIUfqtycepL2TIqxB73NJFpjQ3QAveCuqItsFV41Ys4s130_assertion description "[The mutation in exon 19 of the EGFR gene is in a female and non smoking patient which pathology is SCLC combined adenocarcinoma, and the other is male and smoking patient which pathology is SCLC combined squamous cell carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206907.RAIUfqtycepL2TIqxB73NJFpjQ3QAveCuqItsFV41Ys4s130_provenance.
- NP206907.RAIUfqtycepL2TIqxB73NJFpjQ3QAveCuqItsFV41Ys4s130_assertion evidence source_evidence_literature NP206907.RAIUfqtycepL2TIqxB73NJFpjQ3QAveCuqItsFV41Ys4s130_provenance.
- NP206907.RAIUfqtycepL2TIqxB73NJFpjQ3QAveCuqItsFV41Ys4s130_assertion SIO_000772 22103903 NP206907.RAIUfqtycepL2TIqxB73NJFpjQ3QAveCuqItsFV41Ys4s130_provenance.
- NP206907.RAIUfqtycepL2TIqxB73NJFpjQ3QAveCuqItsFV41Ys4s130_assertion wasDerivedFrom befree-20140225 NP206907.RAIUfqtycepL2TIqxB73NJFpjQ3QAveCuqItsFV41Ys4s130_provenance.
- NP206907.RAIUfqtycepL2TIqxB73NJFpjQ3QAveCuqItsFV41Ys4s130_assertion wasGeneratedBy ECO_0000203 NP206907.RAIUfqtycepL2TIqxB73NJFpjQ3QAveCuqItsFV41Ys4s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP206907.RAIUfqtycepL2TIqxB73NJFpjQ3QAveCuqItsFV41Ys4s130_provenance.