Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP416486.RAv16ZnzQl3DG_G34J4RZT1gOSb_zP4tRQyZf-O0RyQYw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP416486.RAv16ZnzQl3DG_G34J4RZT1gOSb_zP4tRQyZf-O0RyQYw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP416486.RAv16ZnzQl3DG_G34J4RZT1gOSb_zP4tRQyZf-O0RyQYw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP416486.RAv16ZnzQl3DG_G34J4RZT1gOSb_zP4tRQyZf-O0RyQYw130_provenance.
- NP416486.RAv16ZnzQl3DG_G34J4RZT1gOSb_zP4tRQyZf-O0RyQYw130_assertion description "[Allelic loss of 13q14 was observed in 63.2% patients, most of them showing D13S319 and D13S25 deletion; 11% of patients showed TP53 monosomy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP416486.RAv16ZnzQl3DG_G34J4RZT1gOSb_zP4tRQyZf-O0RyQYw130_provenance.
- NP416486.RAv16ZnzQl3DG_G34J4RZT1gOSb_zP4tRQyZf-O0RyQYw130_assertion evidence source_evidence_literature NP416486.RAv16ZnzQl3DG_G34J4RZT1gOSb_zP4tRQyZf-O0RyQYw130_provenance.
- NP416486.RAv16ZnzQl3DG_G34J4RZT1gOSb_zP4tRQyZf-O0RyQYw130_assertion SIO_000772 14553950 NP416486.RAv16ZnzQl3DG_G34J4RZT1gOSb_zP4tRQyZf-O0RyQYw130_provenance.
- NP416486.RAv16ZnzQl3DG_G34J4RZT1gOSb_zP4tRQyZf-O0RyQYw130_assertion wasDerivedFrom befree-2016 NP416486.RAv16ZnzQl3DG_G34J4RZT1gOSb_zP4tRQyZf-O0RyQYw130_provenance.
- NP416486.RAv16ZnzQl3DG_G34J4RZT1gOSb_zP4tRQyZf-O0RyQYw130_assertion wasGeneratedBy ECO_0000203 NP416486.RAv16ZnzQl3DG_G34J4RZT1gOSb_zP4tRQyZf-O0RyQYw130_provenance.
- befree-2016 importedOn "2016-02-19" NP416486.RAv16ZnzQl3DG_G34J4RZT1gOSb_zP4tRQyZf-O0RyQYw130_provenance.