Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP932661.RAWanbNTRCDJTSrqYMSgNHBCWCe3zHEteCwD37vEkw6W0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP932661.RAWanbNTRCDJTSrqYMSgNHBCWCe3zHEteCwD37vEkw6W0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP932661.RAWanbNTRCDJTSrqYMSgNHBCWCe3zHEteCwD37vEkw6W0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP932661.RAWanbNTRCDJTSrqYMSgNHBCWCe3zHEteCwD37vEkw6W0130_provenance.
- NP932661.RAWanbNTRCDJTSrqYMSgNHBCWCe3zHEteCwD37vEkw6W0130_assertion description "[Sensenbrenner syndrome/cranioectodermal dysplasia (CED) is an autosomal-recessive disease that is characterized by craniosynostosis and ectodermal and skeletal abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932661.RAWanbNTRCDJTSrqYMSgNHBCWCe3zHEteCwD37vEkw6W0130_provenance.
- NP932661.RAWanbNTRCDJTSrqYMSgNHBCWCe3zHEteCwD37vEkw6W0130_assertion evidence source_evidence_literature NP932661.RAWanbNTRCDJTSrqYMSgNHBCWCe3zHEteCwD37vEkw6W0130_provenance.
- NP932661.RAWanbNTRCDJTSrqYMSgNHBCWCe3zHEteCwD37vEkw6W0130_assertion SIO_000772 20817137 NP932661.RAWanbNTRCDJTSrqYMSgNHBCWCe3zHEteCwD37vEkw6W0130_provenance.
- NP932661.RAWanbNTRCDJTSrqYMSgNHBCWCe3zHEteCwD37vEkw6W0130_assertion wasDerivedFrom befree-20140225 NP932661.RAWanbNTRCDJTSrqYMSgNHBCWCe3zHEteCwD37vEkw6W0130_provenance.
- NP932661.RAWanbNTRCDJTSrqYMSgNHBCWCe3zHEteCwD37vEkw6W0130_assertion wasGeneratedBy ECO_0000203 NP932661.RAWanbNTRCDJTSrqYMSgNHBCWCe3zHEteCwD37vEkw6W0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP932661.RAWanbNTRCDJTSrqYMSgNHBCWCe3zHEteCwD37vEkw6W0130_provenance.