Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP843078.RAoh8me_0wkKBdEX6TFm6xBgifhNgMRMgi1ZB92iyW2ao130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP843078.RAoh8me_0wkKBdEX6TFm6xBgifhNgMRMgi1ZB92iyW2ao130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP843078.RAoh8me_0wkKBdEX6TFm6xBgifhNgMRMgi1ZB92iyW2ao130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP843078.RAoh8me_0wkKBdEX6TFm6xBgifhNgMRMgi1ZB92iyW2ao130_provenance.
- NP843078.RAoh8me_0wkKBdEX6TFm6xBgifhNgMRMgi1ZB92iyW2ao130_assertion description "[Hence, mutations have now been described in the genes for the 3 subunits of DPM: DPM1, DPM2, and DPM3, whereby DPM2-CDG links the congenital disorders of glycosylation to the congenital muscular dystrophies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP843078.RAoh8me_0wkKBdEX6TFm6xBgifhNgMRMgi1ZB92iyW2ao130_provenance.
- NP843078.RAoh8me_0wkKBdEX6TFm6xBgifhNgMRMgi1ZB92iyW2ao130_assertion evidence source_evidence_literature NP843078.RAoh8me_0wkKBdEX6TFm6xBgifhNgMRMgi1ZB92iyW2ao130_provenance.
- NP843078.RAoh8me_0wkKBdEX6TFm6xBgifhNgMRMgi1ZB92iyW2ao130_assertion SIO_000772 23109149 NP843078.RAoh8me_0wkKBdEX6TFm6xBgifhNgMRMgi1ZB92iyW2ao130_provenance.
- NP843078.RAoh8me_0wkKBdEX6TFm6xBgifhNgMRMgi1ZB92iyW2ao130_assertion wasDerivedFrom befree-20140225 NP843078.RAoh8me_0wkKBdEX6TFm6xBgifhNgMRMgi1ZB92iyW2ao130_provenance.
- NP843078.RAoh8me_0wkKBdEX6TFm6xBgifhNgMRMgi1ZB92iyW2ao130_assertion wasGeneratedBy ECO_0000203 NP843078.RAoh8me_0wkKBdEX6TFm6xBgifhNgMRMgi1ZB92iyW2ao130_provenance.
- befree-20140225 importedOn "2014-02-25" NP843078.RAoh8me_0wkKBdEX6TFm6xBgifhNgMRMgi1ZB92iyW2ao130_provenance.