Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP67713.RAWyHn2VvLnPR-i451Gwrfd_Ds6F7Xgsp-NaLBRj75UIw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP67713.RAWyHn2VvLnPR-i451Gwrfd_Ds6F7Xgsp-NaLBRj75UIw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP67713.RAWyHn2VvLnPR-i451Gwrfd_Ds6F7Xgsp-NaLBRj75UIw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP67713.RAWyHn2VvLnPR-i451Gwrfd_Ds6F7Xgsp-NaLBRj75UIw130_provenance.
- NP67713.RAWyHn2VvLnPR-i451Gwrfd_Ds6F7Xgsp-NaLBRj75UIw130_assertion description "[Association between high von willebrand factor levels and the Thr789Ala vWF gene polymorphism but not with nephropathy in type I diabetes. The GENEDIAB Study Group and the DESIR Study Group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP67713.RAWyHn2VvLnPR-i451Gwrfd_Ds6F7Xgsp-NaLBRj75UIw130_provenance.
- NP67713.RAWyHn2VvLnPR-i451Gwrfd_Ds6F7Xgsp-NaLBRj75UIw130_assertion evidence source_evidence_literature NP67713.RAWyHn2VvLnPR-i451Gwrfd_Ds6F7Xgsp-NaLBRj75UIw130_provenance.
- NP67713.RAWyHn2VvLnPR-i451Gwrfd_Ds6F7Xgsp-NaLBRj75UIw130_assertion SIO_000772 10760079 NP67713.RAWyHn2VvLnPR-i451Gwrfd_Ds6F7Xgsp-NaLBRj75UIw130_provenance.
- NP67713.RAWyHn2VvLnPR-i451Gwrfd_Ds6F7Xgsp-NaLBRj75UIw130_assertion wasDerivedFrom gad-20150221 NP67713.RAWyHn2VvLnPR-i451Gwrfd_Ds6F7Xgsp-NaLBRj75UIw130_provenance.
- NP67713.RAWyHn2VvLnPR-i451Gwrfd_Ds6F7Xgsp-NaLBRj75UIw130_assertion wasGeneratedBy ECO_0000203 NP67713.RAWyHn2VvLnPR-i451Gwrfd_Ds6F7Xgsp-NaLBRj75UIw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP67713.RAWyHn2VvLnPR-i451Gwrfd_Ds6F7Xgsp-NaLBRj75UIw130_provenance.