Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP730138.RAXLKBdng6On-FCVWnd4-B184bGK4KCIh0zdxjDIvbfZM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP730138.RAXLKBdng6On-FCVWnd4-B184bGK4KCIh0zdxjDIvbfZM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP730138.RAXLKBdng6On-FCVWnd4-B184bGK4KCIh0zdxjDIvbfZM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP730138.RAXLKBdng6On-FCVWnd4-B184bGK4KCIh0zdxjDIvbfZM130_provenance.
- NP730138.RAXLKBdng6On-FCVWnd4-B184bGK4KCIh0zdxjDIvbfZM130_assertion description "[SRS and BWS may now be regarded as two diseases caused by opposite (epi)genetic disturbances of the same chromosomal region displaying opposite clinical pictures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP730138.RAXLKBdng6On-FCVWnd4-B184bGK4KCIh0zdxjDIvbfZM130_provenance.
- NP730138.RAXLKBdng6On-FCVWnd4-B184bGK4KCIh0zdxjDIvbfZM130_assertion evidence source_evidence_literature NP730138.RAXLKBdng6On-FCVWnd4-B184bGK4KCIh0zdxjDIvbfZM130_provenance.
- NP730138.RAXLKBdng6On-FCVWnd4-B184bGK4KCIh0zdxjDIvbfZM130_assertion SIO_000772 16236811 NP730138.RAXLKBdng6On-FCVWnd4-B184bGK4KCIh0zdxjDIvbfZM130_provenance.
- NP730138.RAXLKBdng6On-FCVWnd4-B184bGK4KCIh0zdxjDIvbfZM130_assertion wasDerivedFrom befree-20150227 NP730138.RAXLKBdng6On-FCVWnd4-B184bGK4KCIh0zdxjDIvbfZM130_provenance.
- NP730138.RAXLKBdng6On-FCVWnd4-B184bGK4KCIh0zdxjDIvbfZM130_assertion wasGeneratedBy ECO_0000203 NP730138.RAXLKBdng6On-FCVWnd4-B184bGK4KCIh0zdxjDIvbfZM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP730138.RAXLKBdng6On-FCVWnd4-B184bGK4KCIh0zdxjDIvbfZM130_provenance.