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- NP1058885.RAL5KFqCAoRud3JQNwsegz6DqenniaJa0oCVW9rSWwsuk130_assertion type Assertion NP1058885.RAL5KFqCAoRud3JQNwsegz6DqenniaJa0oCVW9rSWwsuk130_head.
- NP1058885.RAL5KFqCAoRud3JQNwsegz6DqenniaJa0oCVW9rSWwsuk130_assertion wasGeneratedBy ECO_0000203 NP1058885.RAL5KFqCAoRud3JQNwsegz6DqenniaJa0oCVW9rSWwsuk130_provenance.
- NP1058885.RAL5KFqCAoRud3JQNwsegz6DqenniaJa0oCVW9rSWwsuk130_assertion wasDerivedFrom befree-2016 NP1058885.RAL5KFqCAoRud3JQNwsegz6DqenniaJa0oCVW9rSWwsuk130_provenance.
- NP1058885.RAL5KFqCAoRud3JQNwsegz6DqenniaJa0oCVW9rSWwsuk130_assertion SIO_000772 23470840 NP1058885.RAL5KFqCAoRud3JQNwsegz6DqenniaJa0oCVW9rSWwsuk130_provenance.
- NP1058885.RAL5KFqCAoRud3JQNwsegz6DqenniaJa0oCVW9rSWwsuk130_assertion evidence source_evidence_literature NP1058885.RAL5KFqCAoRud3JQNwsegz6DqenniaJa0oCVW9rSWwsuk130_provenance.
- NP1058885.RAL5KFqCAoRud3JQNwsegz6DqenniaJa0oCVW9rSWwsuk130_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." NP1058885.RAL5KFqCAoRud3JQNwsegz6DqenniaJa0oCVW9rSWwsuk130_provenance.