Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP155863.RABls_kO5IOUi1GFbyTy32nsaxRgDYHF218Wy8tYc3_2k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP155863.RABls_kO5IOUi1GFbyTy32nsaxRgDYHF218Wy8tYc3_2k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP155863.RABls_kO5IOUi1GFbyTy32nsaxRgDYHF218Wy8tYc3_2k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP155863.RABls_kO5IOUi1GFbyTy32nsaxRgDYHF218Wy8tYc3_2k130_provenance.
- NP155863.RABls_kO5IOUi1GFbyTy32nsaxRgDYHF218Wy8tYc3_2k130_assertion description "[Fusion genes of several variant translocations have been reported in ABC, including a case with t(17;17) and COL1A1-USP6 fusion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP155863.RABls_kO5IOUi1GFbyTy32nsaxRgDYHF218Wy8tYc3_2k130_provenance.
- NP155863.RABls_kO5IOUi1GFbyTy32nsaxRgDYHF218Wy8tYc3_2k130_assertion evidence source_evidence_literature NP155863.RABls_kO5IOUi1GFbyTy32nsaxRgDYHF218Wy8tYc3_2k130_provenance.
- NP155863.RABls_kO5IOUi1GFbyTy32nsaxRgDYHF218Wy8tYc3_2k130_assertion SIO_000772 18068538 NP155863.RABls_kO5IOUi1GFbyTy32nsaxRgDYHF218Wy8tYc3_2k130_provenance.
- NP155863.RABls_kO5IOUi1GFbyTy32nsaxRgDYHF218Wy8tYc3_2k130_assertion wasDerivedFrom befree-20140225 NP155863.RABls_kO5IOUi1GFbyTy32nsaxRgDYHF218Wy8tYc3_2k130_provenance.
- NP155863.RABls_kO5IOUi1GFbyTy32nsaxRgDYHF218Wy8tYc3_2k130_assertion wasGeneratedBy ECO_0000203 NP155863.RABls_kO5IOUi1GFbyTy32nsaxRgDYHF218Wy8tYc3_2k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP155863.RABls_kO5IOUi1GFbyTy32nsaxRgDYHF218Wy8tYc3_2k130_provenance.