Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP601622.RAyMBJuTEZEA1G7rcpN-pJz-6_yFdX5NqWbHD2P5CjI6g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP601622.RAyMBJuTEZEA1G7rcpN-pJz-6_yFdX5NqWbHD2P5CjI6g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP601622.RAyMBJuTEZEA1G7rcpN-pJz-6_yFdX5NqWbHD2P5CjI6g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP601622.RAyMBJuTEZEA1G7rcpN-pJz-6_yFdX5NqWbHD2P5CjI6g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP601622.RAyMBJuTEZEA1G7rcpN-pJz-6_yFdX5NqWbHD2P5CjI6g130_provenance.
- NP601622.RAyMBJuTEZEA1G7rcpN-pJz-6_yFdX5NqWbHD2P5CjI6g130_assertion wasGeneratedBy ECO_0000203 NP601622.RAyMBJuTEZEA1G7rcpN-pJz-6_yFdX5NqWbHD2P5CjI6g130_provenance.
- NP601622.RAyMBJuTEZEA1G7rcpN-pJz-6_yFdX5NqWbHD2P5CjI6g130_assertion wasDerivedFrom befree-20150227 NP601622.RAyMBJuTEZEA1G7rcpN-pJz-6_yFdX5NqWbHD2P5CjI6g130_provenance.
- NP601622.RAyMBJuTEZEA1G7rcpN-pJz-6_yFdX5NqWbHD2P5CjI6g130_assertion SIO_000772 21233288 NP601622.RAyMBJuTEZEA1G7rcpN-pJz-6_yFdX5NqWbHD2P5CjI6g130_provenance.
- NP601622.RAyMBJuTEZEA1G7rcpN-pJz-6_yFdX5NqWbHD2P5CjI6g130_assertion evidence source_evidence_literature NP601622.RAyMBJuTEZEA1G7rcpN-pJz-6_yFdX5NqWbHD2P5CjI6g130_provenance.
- NP601622.RAyMBJuTEZEA1G7rcpN-pJz-6_yFdX5NqWbHD2P5CjI6g130_assertion description "[Mutation of the inositol polyphosphate 5-phosphatase OCRL1 results in two disorders in humans, namely Lowe syndrome (characterized by ocular, nervous system, and renal defects) and type 2 Dent disease (in which only the renal symptoms are evident).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601622.RAyMBJuTEZEA1G7rcpN-pJz-6_yFdX5NqWbHD2P5CjI6g130_provenance.