Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP384677.RAs2oVSDpocMAQG23pVqSdntcIO-2vQlXqHd3uSajB50k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP384677.RAs2oVSDpocMAQG23pVqSdntcIO-2vQlXqHd3uSajB50k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP384677.RAs2oVSDpocMAQG23pVqSdntcIO-2vQlXqHd3uSajB50k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP384677.RAs2oVSDpocMAQG23pVqSdntcIO-2vQlXqHd3uSajB50k130_provenance.
- NP384677.RAs2oVSDpocMAQG23pVqSdntcIO-2vQlXqHd3uSajB50k130_assertion description "[Human association studies show that K8/K18 germline heterozygous mutations predispose to end-stage liver disease of multiple etiologies ( approximately 3 fold increased risk), and to liver disease progression in patients with chronic hepatitis C infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP384677.RAs2oVSDpocMAQG23pVqSdntcIO-2vQlXqHd3uSajB50k130_provenance.
- NP384677.RAs2oVSDpocMAQG23pVqSdntcIO-2vQlXqHd3uSajB50k130_assertion evidence source_evidence_literature NP384677.RAs2oVSDpocMAQG23pVqSdntcIO-2vQlXqHd3uSajB50k130_provenance.
- NP384677.RAs2oVSDpocMAQG23pVqSdntcIO-2vQlXqHd3uSajB50k130_assertion SIO_000772 17969036 NP384677.RAs2oVSDpocMAQG23pVqSdntcIO-2vQlXqHd3uSajB50k130_provenance.
- NP384677.RAs2oVSDpocMAQG23pVqSdntcIO-2vQlXqHd3uSajB50k130_assertion wasDerivedFrom befree-20140225 NP384677.RAs2oVSDpocMAQG23pVqSdntcIO-2vQlXqHd3uSajB50k130_provenance.
- NP384677.RAs2oVSDpocMAQG23pVqSdntcIO-2vQlXqHd3uSajB50k130_assertion wasGeneratedBy ECO_0000203 NP384677.RAs2oVSDpocMAQG23pVqSdntcIO-2vQlXqHd3uSajB50k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP384677.RAs2oVSDpocMAQG23pVqSdntcIO-2vQlXqHd3uSajB50k130_provenance.