Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP778360.RAAvvCdW2GmDE1D-HsdVFfJyv_JbsrLl8IGbunfNl3M0A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP778360.RAAvvCdW2GmDE1D-HsdVFfJyv_JbsrLl8IGbunfNl3M0A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP778360.RAAvvCdW2GmDE1D-HsdVFfJyv_JbsrLl8IGbunfNl3M0A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP778360.RAAvvCdW2GmDE1D-HsdVFfJyv_JbsrLl8IGbunfNl3M0A130_provenance.
- NP778360.RAAvvCdW2GmDE1D-HsdVFfJyv_JbsrLl8IGbunfNl3M0A130_assertion wasGeneratedBy ECO_0000203 NP778360.RAAvvCdW2GmDE1D-HsdVFfJyv_JbsrLl8IGbunfNl3M0A130_provenance.
- NP778360.RAAvvCdW2GmDE1D-HsdVFfJyv_JbsrLl8IGbunfNl3M0A130_assertion wasDerivedFrom befree-20140225 NP778360.RAAvvCdW2GmDE1D-HsdVFfJyv_JbsrLl8IGbunfNl3M0A130_provenance.
- NP778360.RAAvvCdW2GmDE1D-HsdVFfJyv_JbsrLl8IGbunfNl3M0A130_assertion SIO_000772 7723630 NP778360.RAAvvCdW2GmDE1D-HsdVFfJyv_JbsrLl8IGbunfNl3M0A130_provenance.
- NP778360.RAAvvCdW2GmDE1D-HsdVFfJyv_JbsrLl8IGbunfNl3M0A130_assertion evidence source_evidence_literature NP778360.RAAvvCdW2GmDE1D-HsdVFfJyv_JbsrLl8IGbunfNl3M0A130_provenance.
- NP778360.RAAvvCdW2GmDE1D-HsdVFfJyv_JbsrLl8IGbunfNl3M0A130_assertion description "[Only two out of a sample of 48 pedigrees (particularly the early onset FAD 4 kindred) contributed noticeably to evidence of linkage at the D21S16/13 and S1/S11 loci in the chromosomal region 21q21 [75].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778360.RAAvvCdW2GmDE1D-HsdVFfJyv_JbsrLl8IGbunfNl3M0A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP778360.RAAvvCdW2GmDE1D-HsdVFfJyv_JbsrLl8IGbunfNl3M0A130_provenance.