Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP397271.RAn4Pq76EFSFPr6hNG8mOjEs02P25RjymkLDrjwYQSS3I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP397271.RAn4Pq76EFSFPr6hNG8mOjEs02P25RjymkLDrjwYQSS3I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP397271.RAn4Pq76EFSFPr6hNG8mOjEs02P25RjymkLDrjwYQSS3I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP397271.RAn4Pq76EFSFPr6hNG8mOjEs02P25RjymkLDrjwYQSS3I130_provenance.
- NP397271.RAn4Pq76EFSFPr6hNG8mOjEs02P25RjymkLDrjwYQSS3I130_assertion description "[CFCS is genetically heterogeneous and mutations in the KRAS, BRAF, MAP2K1 (MEK1) and MAP2K2 (MEK2) genes, encoding for components of the RAS-mitogen activated protein kinase (MAPK) signaling pathway, have been identified in up to 90% of cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP397271.RAn4Pq76EFSFPr6hNG8mOjEs02P25RjymkLDrjwYQSS3I130_provenance.
- NP397271.RAn4Pq76EFSFPr6hNG8mOjEs02P25RjymkLDrjwYQSS3I130_assertion evidence source_evidence_literature NP397271.RAn4Pq76EFSFPr6hNG8mOjEs02P25RjymkLDrjwYQSS3I130_provenance.
- NP397271.RAn4Pq76EFSFPr6hNG8mOjEs02P25RjymkLDrjwYQSS3I130_assertion SIO_000772 19156172 NP397271.RAn4Pq76EFSFPr6hNG8mOjEs02P25RjymkLDrjwYQSS3I130_provenance.
- NP397271.RAn4Pq76EFSFPr6hNG8mOjEs02P25RjymkLDrjwYQSS3I130_assertion wasDerivedFrom befree-20140225 NP397271.RAn4Pq76EFSFPr6hNG8mOjEs02P25RjymkLDrjwYQSS3I130_provenance.
- NP397271.RAn4Pq76EFSFPr6hNG8mOjEs02P25RjymkLDrjwYQSS3I130_assertion wasGeneratedBy ECO_0000203 NP397271.RAn4Pq76EFSFPr6hNG8mOjEs02P25RjymkLDrjwYQSS3I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP397271.RAn4Pq76EFSFPr6hNG8mOjEs02P25RjymkLDrjwYQSS3I130_provenance.