Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1085036.RAs4KlxLC3VHD8wt49QvzMcjNSkj-s5r8Kb3tj1bmWNuo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1085036.RAs4KlxLC3VHD8wt49QvzMcjNSkj-s5r8Kb3tj1bmWNuo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1085036.RAs4KlxLC3VHD8wt49QvzMcjNSkj-s5r8Kb3tj1bmWNuo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1085036.RAs4KlxLC3VHD8wt49QvzMcjNSkj-s5r8Kb3tj1bmWNuo130_provenance.
- NP1085036.RAs4KlxLC3VHD8wt49QvzMcjNSkj-s5r8Kb3tj1bmWNuo130_assertion description "[Three SNP alleles in BRD2, Cx-36, and ME2 and microdeletions in 15q13.3, 15q11.2, and 16p13.11 also contribute risk to JME.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1085036.RAs4KlxLC3VHD8wt49QvzMcjNSkj-s5r8Kb3tj1bmWNuo130_provenance.
- NP1085036.RAs4KlxLC3VHD8wt49QvzMcjNSkj-s5r8Kb3tj1bmWNuo130_assertion evidence source_evidence_literature NP1085036.RAs4KlxLC3VHD8wt49QvzMcjNSkj-s5r8Kb3tj1bmWNuo130_provenance.
- NP1085036.RAs4KlxLC3VHD8wt49QvzMcjNSkj-s5r8Kb3tj1bmWNuo130_assertion SIO_000772 23756480 NP1085036.RAs4KlxLC3VHD8wt49QvzMcjNSkj-s5r8Kb3tj1bmWNuo130_provenance.
- NP1085036.RAs4KlxLC3VHD8wt49QvzMcjNSkj-s5r8Kb3tj1bmWNuo130_assertion wasDerivedFrom befree-2016 NP1085036.RAs4KlxLC3VHD8wt49QvzMcjNSkj-s5r8Kb3tj1bmWNuo130_provenance.
- NP1085036.RAs4KlxLC3VHD8wt49QvzMcjNSkj-s5r8Kb3tj1bmWNuo130_assertion wasGeneratedBy ECO_0000203 NP1085036.RAs4KlxLC3VHD8wt49QvzMcjNSkj-s5r8Kb3tj1bmWNuo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1085036.RAs4KlxLC3VHD8wt49QvzMcjNSkj-s5r8Kb3tj1bmWNuo130_provenance.