Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP865441.RAc9R5Bhvftm0MHjxUDUpnFqls5hnCLGRilbP2AiB1v_g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP865441.RAc9R5Bhvftm0MHjxUDUpnFqls5hnCLGRilbP2AiB1v_g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP865441.RAc9R5Bhvftm0MHjxUDUpnFqls5hnCLGRilbP2AiB1v_g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP865441.RAc9R5Bhvftm0MHjxUDUpnFqls5hnCLGRilbP2AiB1v_g130_provenance.
- NP865441.RAc9R5Bhvftm0MHjxUDUpnFqls5hnCLGRilbP2AiB1v_g130_assertion description "[The molecular composition of DAPs was recently elucidated and mutations in two genes encoding DAPs components (CEP164/NPHP15, SCLT1) have been associated with human ciliopathies, namely nephronophthisis and orofaciodigital syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865441.RAc9R5Bhvftm0MHjxUDUpnFqls5hnCLGRilbP2AiB1v_g130_provenance.
- NP865441.RAc9R5Bhvftm0MHjxUDUpnFqls5hnCLGRilbP2AiB1v_g130_assertion evidence source_evidence_literature NP865441.RAc9R5Bhvftm0MHjxUDUpnFqls5hnCLGRilbP2AiB1v_g130_provenance.
- NP865441.RAc9R5Bhvftm0MHjxUDUpnFqls5hnCLGRilbP2AiB1v_g130_assertion SIO_000772 24882706 NP865441.RAc9R5Bhvftm0MHjxUDUpnFqls5hnCLGRilbP2AiB1v_g130_provenance.
- NP865441.RAc9R5Bhvftm0MHjxUDUpnFqls5hnCLGRilbP2AiB1v_g130_assertion wasDerivedFrom befree-20150227 NP865441.RAc9R5Bhvftm0MHjxUDUpnFqls5hnCLGRilbP2AiB1v_g130_provenance.
- NP865441.RAc9R5Bhvftm0MHjxUDUpnFqls5hnCLGRilbP2AiB1v_g130_assertion wasGeneratedBy ECO_0000203 NP865441.RAc9R5Bhvftm0MHjxUDUpnFqls5hnCLGRilbP2AiB1v_g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP865441.RAc9R5Bhvftm0MHjxUDUpnFqls5hnCLGRilbP2AiB1v_g130_provenance.