Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP258812.RAQKNwARPssjSQD7854AfeBtx0g9UTgAc1c-P81bR4FME130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP258812.RAQKNwARPssjSQD7854AfeBtx0g9UTgAc1c-P81bR4FME130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP258812.RAQKNwARPssjSQD7854AfeBtx0g9UTgAc1c-P81bR4FME130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP258812.RAQKNwARPssjSQD7854AfeBtx0g9UTgAc1c-P81bR4FME130_provenance.
- NP258812.RAQKNwARPssjSQD7854AfeBtx0g9UTgAc1c-P81bR4FME130_assertion description "[The enrichment of ERBB2 mutations/fusion in CDH1-mutated ILC (5 of 22, 23%) compared with the 5 ERBB2 mutations in a series of 286 non-CDH1-mutated breast cancers from which the ILC cases were obtained (5 of 286, 2%) was significant (P = 0.0006).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258812.RAQKNwARPssjSQD7854AfeBtx0g9UTgAc1c-P81bR4FME130_provenance.
- NP258812.RAQKNwARPssjSQD7854AfeBtx0g9UTgAc1c-P81bR4FME130_assertion evidence source_evidence_literature NP258812.RAQKNwARPssjSQD7854AfeBtx0g9UTgAc1c-P81bR4FME130_provenance.
- NP258812.RAQKNwARPssjSQD7854AfeBtx0g9UTgAc1c-P81bR4FME130_assertion SIO_000772 23575477 NP258812.RAQKNwARPssjSQD7854AfeBtx0g9UTgAc1c-P81bR4FME130_provenance.
- NP258812.RAQKNwARPssjSQD7854AfeBtx0g9UTgAc1c-P81bR4FME130_assertion wasDerivedFrom befree-20140225 NP258812.RAQKNwARPssjSQD7854AfeBtx0g9UTgAc1c-P81bR4FME130_provenance.
- NP258812.RAQKNwARPssjSQD7854AfeBtx0g9UTgAc1c-P81bR4FME130_assertion wasGeneratedBy ECO_0000203 NP258812.RAQKNwARPssjSQD7854AfeBtx0g9UTgAc1c-P81bR4FME130_provenance.
- befree-20140225 importedOn "2014-02-25" NP258812.RAQKNwARPssjSQD7854AfeBtx0g9UTgAc1c-P81bR4FME130_provenance.