Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP776759.RAl7LvGS-zBxenI4pw8Jjx7wH7vdPWJO6GfHPDfGXZTdg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP776759.RAl7LvGS-zBxenI4pw8Jjx7wH7vdPWJO6GfHPDfGXZTdg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP776759.RAl7LvGS-zBxenI4pw8Jjx7wH7vdPWJO6GfHPDfGXZTdg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP776759.RAl7LvGS-zBxenI4pw8Jjx7wH7vdPWJO6GfHPDfGXZTdg130_provenance.
- NP776759.RAl7LvGS-zBxenI4pw8Jjx7wH7vdPWJO6GfHPDfGXZTdg130_assertion description "[The contribution of CLIP2 haploinsufficiency to the clinical manifestations of the Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776759.RAl7LvGS-zBxenI4pw8Jjx7wH7vdPWJO6GfHPDfGXZTdg130_provenance.
- NP776759.RAl7LvGS-zBxenI4pw8Jjx7wH7vdPWJO6GfHPDfGXZTdg130_assertion evidence source_evidence_literature NP776759.RAl7LvGS-zBxenI4pw8Jjx7wH7vdPWJO6GfHPDfGXZTdg130_provenance.
- NP776759.RAl7LvGS-zBxenI4pw8Jjx7wH7vdPWJO6GfHPDfGXZTdg130_assertion SIO_000772 22608712 NP776759.RAl7LvGS-zBxenI4pw8Jjx7wH7vdPWJO6GfHPDfGXZTdg130_provenance.
- NP776759.RAl7LvGS-zBxenI4pw8Jjx7wH7vdPWJO6GfHPDfGXZTdg130_assertion wasDerivedFrom befree-20150227 NP776759.RAl7LvGS-zBxenI4pw8Jjx7wH7vdPWJO6GfHPDfGXZTdg130_provenance.
- NP776759.RAl7LvGS-zBxenI4pw8Jjx7wH7vdPWJO6GfHPDfGXZTdg130_assertion wasGeneratedBy ECO_0000203 NP776759.RAl7LvGS-zBxenI4pw8Jjx7wH7vdPWJO6GfHPDfGXZTdg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP776759.RAl7LvGS-zBxenI4pw8Jjx7wH7vdPWJO6GfHPDfGXZTdg130_provenance.