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- source_evidence_literature type ECO_0000212 NP488175.RAvHj_y-gYco_HlZlibPR6XC84dX46nHnyW7cuOcfkN18130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP488175.RAvHj_y-gYco_HlZlibPR6XC84dX46nHnyW7cuOcfkN18130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP488175.RAvHj_y-gYco_HlZlibPR6XC84dX46nHnyW7cuOcfkN18130_provenance.
- NP488175.RAvHj_y-gYco_HlZlibPR6XC84dX46nHnyW7cuOcfkN18130_assertion description "[Farber disease is an autosomal recessive disorder caused by lysosomal acid ceramidase (AC) deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP488175.RAvHj_y-gYco_HlZlibPR6XC84dX46nHnyW7cuOcfkN18130_provenance.
- NP488175.RAvHj_y-gYco_HlZlibPR6XC84dX46nHnyW7cuOcfkN18130_assertion evidence source_evidence_literature NP488175.RAvHj_y-gYco_HlZlibPR6XC84dX46nHnyW7cuOcfkN18130_provenance.
- NP488175.RAvHj_y-gYco_HlZlibPR6XC84dX46nHnyW7cuOcfkN18130_assertion SIO_000772 10993717 NP488175.RAvHj_y-gYco_HlZlibPR6XC84dX46nHnyW7cuOcfkN18130_provenance.
- NP488175.RAvHj_y-gYco_HlZlibPR6XC84dX46nHnyW7cuOcfkN18130_assertion wasDerivedFrom befree-20140225 NP488175.RAvHj_y-gYco_HlZlibPR6XC84dX46nHnyW7cuOcfkN18130_provenance.
- NP488175.RAvHj_y-gYco_HlZlibPR6XC84dX46nHnyW7cuOcfkN18130_assertion wasGeneratedBy ECO_0000203 NP488175.RAvHj_y-gYco_HlZlibPR6XC84dX46nHnyW7cuOcfkN18130_provenance.
- befree-20140225 importedOn "2014-02-25" NP488175.RAvHj_y-gYco_HlZlibPR6XC84dX46nHnyW7cuOcfkN18130_provenance.