Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP419014.RAvaNHdXno2rePRMT0tjq39QOJRxj-Hx-7n7ky6W3t_8w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP419014.RAvaNHdXno2rePRMT0tjq39QOJRxj-Hx-7n7ky6W3t_8w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP419014.RAvaNHdXno2rePRMT0tjq39QOJRxj-Hx-7n7ky6W3t_8w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP419014.RAvaNHdXno2rePRMT0tjq39QOJRxj-Hx-7n7ky6W3t_8w130_provenance.
- NP419014.RAvaNHdXno2rePRMT0tjq39QOJRxj-Hx-7n7ky6W3t_8w130_assertion description "[The identification of recurrent cytogenetic abnormalities is hampered by difficulty in culturing tumours and the lack of CD30+ CTCL serial studies comparing genetic changes both at diagnosis and at relapse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419014.RAvaNHdXno2rePRMT0tjq39QOJRxj-Hx-7n7ky6W3t_8w130_provenance.
- NP419014.RAvaNHdXno2rePRMT0tjq39QOJRxj-Hx-7n7ky6W3t_8w130_assertion evidence source_evidence_literature NP419014.RAvaNHdXno2rePRMT0tjq39QOJRxj-Hx-7n7ky6W3t_8w130_provenance.
- NP419014.RAvaNHdXno2rePRMT0tjq39QOJRxj-Hx-7n7ky6W3t_8w130_assertion SIO_000772 14595754 NP419014.RAvaNHdXno2rePRMT0tjq39QOJRxj-Hx-7n7ky6W3t_8w130_provenance.
- NP419014.RAvaNHdXno2rePRMT0tjq39QOJRxj-Hx-7n7ky6W3t_8w130_assertion wasDerivedFrom befree-2016 NP419014.RAvaNHdXno2rePRMT0tjq39QOJRxj-Hx-7n7ky6W3t_8w130_provenance.
- NP419014.RAvaNHdXno2rePRMT0tjq39QOJRxj-Hx-7n7ky6W3t_8w130_assertion wasGeneratedBy ECO_0000203 NP419014.RAvaNHdXno2rePRMT0tjq39QOJRxj-Hx-7n7ky6W3t_8w130_provenance.
- befree-2016 importedOn "2016-02-19" NP419014.RAvaNHdXno2rePRMT0tjq39QOJRxj-Hx-7n7ky6W3t_8w130_provenance.