Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1266906.RAD8rwff4I_SxO9ku1TIy7AH960fH_iGai8SucHwqg8Hc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1266906.RAD8rwff4I_SxO9ku1TIy7AH960fH_iGai8SucHwqg8Hc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1266906.RAD8rwff4I_SxO9ku1TIy7AH960fH_iGai8SucHwqg8Hc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1266906.RAD8rwff4I_SxO9ku1TIy7AH960fH_iGai8SucHwqg8Hc130_provenance.
- NP1266906.RAD8rwff4I_SxO9ku1TIy7AH960fH_iGai8SucHwqg8Hc130_assertion description "[The loss of Ctnnd2, the gene encoding ?-catenin, has been associated with the intellectual disability observed in the cri du chat syndrome, suggesting that the functional roles of ?-catenin are vital for neuronal integrity and higher order functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266906.RAD8rwff4I_SxO9ku1TIy7AH960fH_iGai8SucHwqg8Hc130_provenance.
- NP1266906.RAD8rwff4I_SxO9ku1TIy7AH960fH_iGai8SucHwqg8Hc130_assertion evidence source_evidence_literature NP1266906.RAD8rwff4I_SxO9ku1TIy7AH960fH_iGai8SucHwqg8Hc130_provenance.
- NP1266906.RAD8rwff4I_SxO9ku1TIy7AH960fH_iGai8SucHwqg8Hc130_assertion SIO_000772 25724647 NP1266906.RAD8rwff4I_SxO9ku1TIy7AH960fH_iGai8SucHwqg8Hc130_provenance.
- NP1266906.RAD8rwff4I_SxO9ku1TIy7AH960fH_iGai8SucHwqg8Hc130_assertion wasDerivedFrom befree-2016 NP1266906.RAD8rwff4I_SxO9ku1TIy7AH960fH_iGai8SucHwqg8Hc130_provenance.
- NP1266906.RAD8rwff4I_SxO9ku1TIy7AH960fH_iGai8SucHwqg8Hc130_assertion wasGeneratedBy ECO_0000203 NP1266906.RAD8rwff4I_SxO9ku1TIy7AH960fH_iGai8SucHwqg8Hc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1266906.RAD8rwff4I_SxO9ku1TIy7AH960fH_iGai8SucHwqg8Hc130_provenance.