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- source_evidence_literature type ECO_0000212 NP290227.RAinE92V5Nlzbvydw-lhM2dRwS45nJ2dQnDa_AdMdUbMU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP290227.RAinE92V5Nlzbvydw-lhM2dRwS45nJ2dQnDa_AdMdUbMU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP290227.RAinE92V5Nlzbvydw-lhM2dRwS45nJ2dQnDa_AdMdUbMU130_provenance.
- NP290227.RAinE92V5Nlzbvydw-lhM2dRwS45nJ2dQnDa_AdMdUbMU130_assertion description "[In summary, we have identified defects in IFT172 as a cause of complex ATD and MZSDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP290227.RAinE92V5Nlzbvydw-lhM2dRwS45nJ2dQnDa_AdMdUbMU130_provenance.
- NP290227.RAinE92V5Nlzbvydw-lhM2dRwS45nJ2dQnDa_AdMdUbMU130_assertion evidence source_evidence_literature NP290227.RAinE92V5Nlzbvydw-lhM2dRwS45nJ2dQnDa_AdMdUbMU130_provenance.
- NP290227.RAinE92V5Nlzbvydw-lhM2dRwS45nJ2dQnDa_AdMdUbMU130_assertion SIO_000772 24140113 NP290227.RAinE92V5Nlzbvydw-lhM2dRwS45nJ2dQnDa_AdMdUbMU130_provenance.
- NP290227.RAinE92V5Nlzbvydw-lhM2dRwS45nJ2dQnDa_AdMdUbMU130_assertion wasDerivedFrom befree-20140225 NP290227.RAinE92V5Nlzbvydw-lhM2dRwS45nJ2dQnDa_AdMdUbMU130_provenance.
- NP290227.RAinE92V5Nlzbvydw-lhM2dRwS45nJ2dQnDa_AdMdUbMU130_assertion wasGeneratedBy ECO_0000203 NP290227.RAinE92V5Nlzbvydw-lhM2dRwS45nJ2dQnDa_AdMdUbMU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP290227.RAinE92V5Nlzbvydw-lhM2dRwS45nJ2dQnDa_AdMdUbMU130_provenance.