Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP868951.RAE-3On6J6YQhz_pMiCmnDdZkWByqwtdWs8lzHRMrbL10130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP868951.RAE-3On6J6YQhz_pMiCmnDdZkWByqwtdWs8lzHRMrbL10130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868951.RAE-3On6J6YQhz_pMiCmnDdZkWByqwtdWs8lzHRMrbL10130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868951.RAE-3On6J6YQhz_pMiCmnDdZkWByqwtdWs8lzHRMrbL10130_provenance.
- NP868951.RAE-3On6J6YQhz_pMiCmnDdZkWByqwtdWs8lzHRMrbL10130_assertion wasGeneratedBy ECO_0000203 NP868951.RAE-3On6J6YQhz_pMiCmnDdZkWByqwtdWs8lzHRMrbL10130_provenance.
- NP868951.RAE-3On6J6YQhz_pMiCmnDdZkWByqwtdWs8lzHRMrbL10130_assertion wasDerivedFrom befree-20140225 NP868951.RAE-3On6J6YQhz_pMiCmnDdZkWByqwtdWs8lzHRMrbL10130_provenance.
- NP868951.RAE-3On6J6YQhz_pMiCmnDdZkWByqwtdWs8lzHRMrbL10130_assertion SIO_000772 10814714 NP868951.RAE-3On6J6YQhz_pMiCmnDdZkWByqwtdWs8lzHRMrbL10130_provenance.
- NP868951.RAE-3On6J6YQhz_pMiCmnDdZkWByqwtdWs8lzHRMrbL10130_assertion evidence source_evidence_literature NP868951.RAE-3On6J6YQhz_pMiCmnDdZkWByqwtdWs8lzHRMrbL10130_provenance.
- NP868951.RAE-3On6J6YQhz_pMiCmnDdZkWByqwtdWs8lzHRMrbL10130_assertion description "[We have examined the mutational status of the GPC3 and GPC4 genes in one patient with Perlman syndrome, three patients with overgrowth without syndrome diagnosis, ten unrelated SGBS-patients and 11 BWS patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868951.RAE-3On6J6YQhz_pMiCmnDdZkWByqwtdWs8lzHRMrbL10130_provenance.
- befree-20140225 importedOn "2014-02-25" NP868951.RAE-3On6J6YQhz_pMiCmnDdZkWByqwtdWs8lzHRMrbL10130_provenance.