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- NP893.RAIOR-6wePndu_NLyUi-teH48jm8bhW6YvzEGwKLTr_Jw130_assertion type Assertion NP893.RAIOR-6wePndu_NLyUi-teH48jm8bhW6YvzEGwKLTr_Jw130_head.
- NP893.RAIOR-6wePndu_NLyUi-teH48jm8bhW6YvzEGwKLTr_Jw130_assertion description "[Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP893.RAIOR-6wePndu_NLyUi-teH48jm8bhW6YvzEGwKLTr_Jw130_provenance.
- NP893.RAIOR-6wePndu_NLyUi-teH48jm8bhW6YvzEGwKLTr_Jw130_assertion evidence source_evidence_curated NP893.RAIOR-6wePndu_NLyUi-teH48jm8bhW6YvzEGwKLTr_Jw130_provenance.
- NP893.RAIOR-6wePndu_NLyUi-teH48jm8bhW6YvzEGwKLTr_Jw130_assertion SIO_000772 10878661 NP893.RAIOR-6wePndu_NLyUi-teH48jm8bhW6YvzEGwKLTr_Jw130_provenance.
- NP893.RAIOR-6wePndu_NLyUi-teH48jm8bhW6YvzEGwKLTr_Jw130_assertion wasDerivedFrom uniprot-2016 NP893.RAIOR-6wePndu_NLyUi-teH48jm8bhW6YvzEGwKLTr_Jw130_provenance.
- NP893.RAIOR-6wePndu_NLyUi-teH48jm8bhW6YvzEGwKLTr_Jw130_assertion wasGeneratedBy ECO_0000218 NP893.RAIOR-6wePndu_NLyUi-teH48jm8bhW6YvzEGwKLTr_Jw130_provenance.