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- NP601622.RAyMBJuTEZEA1G7rcpN-pJz-6_yFdX5NqWbHD2P5CjI6g130_assertion type Assertion NP601622.RAyMBJuTEZEA1G7rcpN-pJz-6_yFdX5NqWbHD2P5CjI6g130_head.
- 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.