Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP860206.RAdaqlrxUoFwu5T_Sv0thCc-xkcM3Ks0r8CX1gpIBFAyA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP860206.RAdaqlrxUoFwu5T_Sv0thCc-xkcM3Ks0r8CX1gpIBFAyA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP860206.RAdaqlrxUoFwu5T_Sv0thCc-xkcM3Ks0r8CX1gpIBFAyA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP860206.RAdaqlrxUoFwu5T_Sv0thCc-xkcM3Ks0r8CX1gpIBFAyA130_provenance.
- NP860206.RAdaqlrxUoFwu5T_Sv0thCc-xkcM3Ks0r8CX1gpIBFAyA130_assertion wasGeneratedBy ECO_0000203 NP860206.RAdaqlrxUoFwu5T_Sv0thCc-xkcM3Ks0r8CX1gpIBFAyA130_provenance.
- NP860206.RAdaqlrxUoFwu5T_Sv0thCc-xkcM3Ks0r8CX1gpIBFAyA130_assertion wasDerivedFrom befree-20140225 NP860206.RAdaqlrxUoFwu5T_Sv0thCc-xkcM3Ks0r8CX1gpIBFAyA130_provenance.
- NP860206.RAdaqlrxUoFwu5T_Sv0thCc-xkcM3Ks0r8CX1gpIBFAyA130_assertion SIO_000772 17564967 NP860206.RAdaqlrxUoFwu5T_Sv0thCc-xkcM3Ks0r8CX1gpIBFAyA130_provenance.
- NP860206.RAdaqlrxUoFwu5T_Sv0thCc-xkcM3Ks0r8CX1gpIBFAyA130_assertion evidence source_evidence_literature NP860206.RAdaqlrxUoFwu5T_Sv0thCc-xkcM3Ks0r8CX1gpIBFAyA130_provenance.
- NP860206.RAdaqlrxUoFwu5T_Sv0thCc-xkcM3Ks0r8CX1gpIBFAyA130_assertion description "[Mutations in the CEP290 gene were recently identified in families with the MTS-related neurological features, many of which showed oculo-renal involvement typical of Senior-Loken syndrome (JSRD-SLS phenotype).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP860206.RAdaqlrxUoFwu5T_Sv0thCc-xkcM3Ks0r8CX1gpIBFAyA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP860206.RAdaqlrxUoFwu5T_Sv0thCc-xkcM3Ks0r8CX1gpIBFAyA130_provenance.