Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1058887.RAznO_nbBBBZcGho_eR8RM6iFV1t1zL7TjB_fxRPlwb5I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1058887.RAznO_nbBBBZcGho_eR8RM6iFV1t1zL7TjB_fxRPlwb5I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1058887.RAznO_nbBBBZcGho_eR8RM6iFV1t1zL7TjB_fxRPlwb5I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1058887.RAznO_nbBBBZcGho_eR8RM6iFV1t1zL7TjB_fxRPlwb5I130_provenance.
- befree-2016 importedOn "2016-02-19" NP1058887.RAznO_nbBBBZcGho_eR8RM6iFV1t1zL7TjB_fxRPlwb5I130_provenance.
- NP1058887.RAznO_nbBBBZcGho_eR8RM6iFV1t1zL7TjB_fxRPlwb5I130_assertion wasGeneratedBy ECO_0000203 NP1058887.RAznO_nbBBBZcGho_eR8RM6iFV1t1zL7TjB_fxRPlwb5I130_provenance.
- NP1058887.RAznO_nbBBBZcGho_eR8RM6iFV1t1zL7TjB_fxRPlwb5I130_assertion wasDerivedFrom befree-2016 NP1058887.RAznO_nbBBBZcGho_eR8RM6iFV1t1zL7TjB_fxRPlwb5I130_provenance.
- NP1058887.RAznO_nbBBBZcGho_eR8RM6iFV1t1zL7TjB_fxRPlwb5I130_assertion SIO_000772 23470840 NP1058887.RAznO_nbBBBZcGho_eR8RM6iFV1t1zL7TjB_fxRPlwb5I130_provenance.
- NP1058887.RAznO_nbBBBZcGho_eR8RM6iFV1t1zL7TjB_fxRPlwb5I130_assertion evidence source_evidence_literature NP1058887.RAznO_nbBBBZcGho_eR8RM6iFV1t1zL7TjB_fxRPlwb5I130_provenance.
- NP1058887.RAznO_nbBBBZcGho_eR8RM6iFV1t1zL7TjB_fxRPlwb5I130_assertion description "[We sought to characterize cognition in individuals with germline PTEN mutations (n = 23) as well as in PTEN mutation-negative individuals with classic Cowden syndrome or Bannayan-Riley-Ruvalcaba syndrome (n = 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1058887.RAznO_nbBBBZcGho_eR8RM6iFV1t1zL7TjB_fxRPlwb5I130_provenance.