Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP673479.RAvHlhUs2-kppuat6J25cDV9zKiuQlidlxu8kvvlBterE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP673479.RAvHlhUs2-kppuat6J25cDV9zKiuQlidlxu8kvvlBterE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP673479.RAvHlhUs2-kppuat6J25cDV9zKiuQlidlxu8kvvlBterE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP673479.RAvHlhUs2-kppuat6J25cDV9zKiuQlidlxu8kvvlBterE130_provenance.
- NP673479.RAvHlhUs2-kppuat6J25cDV9zKiuQlidlxu8kvvlBterE130_assertion description "[Comparison of this patient's dysmorphic features with previously reported cases of ring 3 or deletion 3p suggests a clinical syndrome derived mainly from deletion of 3p26 leads to pter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP673479.RAvHlhUs2-kppuat6J25cDV9zKiuQlidlxu8kvvlBterE130_provenance.
- NP673479.RAvHlhUs2-kppuat6J25cDV9zKiuQlidlxu8kvvlBterE130_assertion evidence source_evidence_literature NP673479.RAvHlhUs2-kppuat6J25cDV9zKiuQlidlxu8kvvlBterE130_provenance.
- NP673479.RAvHlhUs2-kppuat6J25cDV9zKiuQlidlxu8kvvlBterE130_assertion SIO_000772 7154048 NP673479.RAvHlhUs2-kppuat6J25cDV9zKiuQlidlxu8kvvlBterE130_provenance.
- NP673479.RAvHlhUs2-kppuat6J25cDV9zKiuQlidlxu8kvvlBterE130_assertion wasDerivedFrom befree-20150227 NP673479.RAvHlhUs2-kppuat6J25cDV9zKiuQlidlxu8kvvlBterE130_provenance.
- NP673479.RAvHlhUs2-kppuat6J25cDV9zKiuQlidlxu8kvvlBterE130_assertion wasGeneratedBy ECO_0000203 NP673479.RAvHlhUs2-kppuat6J25cDV9zKiuQlidlxu8kvvlBterE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP673479.RAvHlhUs2-kppuat6J25cDV9zKiuQlidlxu8kvvlBterE130_provenance.