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- source_evidence_literature type ECO_0000212 NP831471.RAXGiPRHlLAh_mu0p1NcrKUhx8tQxbuavRdoARYwHtUzk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP831471.RAXGiPRHlLAh_mu0p1NcrKUhx8tQxbuavRdoARYwHtUzk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP831471.RAXGiPRHlLAh_mu0p1NcrKUhx8tQxbuavRdoARYwHtUzk130_provenance.
- NP831471.RAXGiPRHlLAh_mu0p1NcrKUhx8tQxbuavRdoARYwHtUzk130_assertion description "[The novel findings included a set of genes (DCDC2, DYX1C1, KIAA0319) related to a neurological disease dyslexia suggesting their potential involvement in ciliary functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831471.RAXGiPRHlLAh_mu0p1NcrKUhx8tQxbuavRdoARYwHtUzk130_provenance.
- NP831471.RAXGiPRHlLAh_mu0p1NcrKUhx8tQxbuavRdoARYwHtUzk130_assertion evidence source_evidence_literature NP831471.RAXGiPRHlLAh_mu0p1NcrKUhx8tQxbuavRdoARYwHtUzk130_provenance.
- NP831471.RAXGiPRHlLAh_mu0p1NcrKUhx8tQxbuavRdoARYwHtUzk130_assertion SIO_000772 22558177 NP831471.RAXGiPRHlLAh_mu0p1NcrKUhx8tQxbuavRdoARYwHtUzk130_provenance.
- NP831471.RAXGiPRHlLAh_mu0p1NcrKUhx8tQxbuavRdoARYwHtUzk130_assertion wasDerivedFrom befree-20150227 NP831471.RAXGiPRHlLAh_mu0p1NcrKUhx8tQxbuavRdoARYwHtUzk130_provenance.
- NP831471.RAXGiPRHlLAh_mu0p1NcrKUhx8tQxbuavRdoARYwHtUzk130_assertion wasGeneratedBy ECO_0000203 NP831471.RAXGiPRHlLAh_mu0p1NcrKUhx8tQxbuavRdoARYwHtUzk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP831471.RAXGiPRHlLAh_mu0p1NcrKUhx8tQxbuavRdoARYwHtUzk130_provenance.