Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1327671.RA5KcBG9OfdAH6C2mxqBJ9sfwm1mGuPnElHnq5-CdaCcs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1327671.RA5KcBG9OfdAH6C2mxqBJ9sfwm1mGuPnElHnq5-CdaCcs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1327671.RA5KcBG9OfdAH6C2mxqBJ9sfwm1mGuPnElHnq5-CdaCcs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1327671.RA5KcBG9OfdAH6C2mxqBJ9sfwm1mGuPnElHnq5-CdaCcs130_provenance.
- NP1327671.RA5KcBG9OfdAH6C2mxqBJ9sfwm1mGuPnElHnq5-CdaCcs130_assertion description "[No recombination events were noted with the following markers within the DMD locus: 5'DYS II, intron 44, DXS997, and intron 50.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327671.RA5KcBG9OfdAH6C2mxqBJ9sfwm1mGuPnElHnq5-CdaCcs130_provenance.
- NP1327671.RA5KcBG9OfdAH6C2mxqBJ9sfwm1mGuPnElHnq5-CdaCcs130_assertion evidence source_evidence_literature NP1327671.RA5KcBG9OfdAH6C2mxqBJ9sfwm1mGuPnElHnq5-CdaCcs130_provenance.
- NP1327671.RA5KcBG9OfdAH6C2mxqBJ9sfwm1mGuPnElHnq5-CdaCcs130_assertion SIO_000772 7942846 NP1327671.RA5KcBG9OfdAH6C2mxqBJ9sfwm1mGuPnElHnq5-CdaCcs130_provenance.
- NP1327671.RA5KcBG9OfdAH6C2mxqBJ9sfwm1mGuPnElHnq5-CdaCcs130_assertion wasDerivedFrom befree-2016 NP1327671.RA5KcBG9OfdAH6C2mxqBJ9sfwm1mGuPnElHnq5-CdaCcs130_provenance.
- NP1327671.RA5KcBG9OfdAH6C2mxqBJ9sfwm1mGuPnElHnq5-CdaCcs130_assertion wasGeneratedBy ECO_0000203 NP1327671.RA5KcBG9OfdAH6C2mxqBJ9sfwm1mGuPnElHnq5-CdaCcs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1327671.RA5KcBG9OfdAH6C2mxqBJ9sfwm1mGuPnElHnq5-CdaCcs130_provenance.