Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP381580.RACq0IKIuTQCn8X43UP9HnFOvapvigUj1INHw-_gS3jCQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP381580.RACq0IKIuTQCn8X43UP9HnFOvapvigUj1INHw-_gS3jCQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381580.RACq0IKIuTQCn8X43UP9HnFOvapvigUj1INHw-_gS3jCQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381580.RACq0IKIuTQCn8X43UP9HnFOvapvigUj1INHw-_gS3jCQ130_provenance.
- NP381580.RACq0IKIuTQCn8X43UP9HnFOvapvigUj1INHw-_gS3jCQ130_assertion description "[Although hidden genetic changes have been found in some trisomies, for example, mutations in KIT in acute myelocytic leukemia (AML) with +4 and in MET in hereditary papillary kidney carcinoma with trisomy 7, none associated with +8 have so far been discovered.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381580.RACq0IKIuTQCn8X43UP9HnFOvapvigUj1INHw-_gS3jCQ130_provenance.
- NP381580.RACq0IKIuTQCn8X43UP9HnFOvapvigUj1INHw-_gS3jCQ130_assertion evidence source_evidence_literature NP381580.RACq0IKIuTQCn8X43UP9HnFOvapvigUj1INHw-_gS3jCQ130_provenance.
- NP381580.RACq0IKIuTQCn8X43UP9HnFOvapvigUj1INHw-_gS3jCQ130_assertion SIO_000772 12550762 NP381580.RACq0IKIuTQCn8X43UP9HnFOvapvigUj1INHw-_gS3jCQ130_provenance.
- NP381580.RACq0IKIuTQCn8X43UP9HnFOvapvigUj1INHw-_gS3jCQ130_assertion wasDerivedFrom befree-2016 NP381580.RACq0IKIuTQCn8X43UP9HnFOvapvigUj1INHw-_gS3jCQ130_provenance.
- NP381580.RACq0IKIuTQCn8X43UP9HnFOvapvigUj1INHw-_gS3jCQ130_assertion wasGeneratedBy ECO_0000203 NP381580.RACq0IKIuTQCn8X43UP9HnFOvapvigUj1INHw-_gS3jCQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP381580.RACq0IKIuTQCn8X43UP9HnFOvapvigUj1INHw-_gS3jCQ130_provenance.