Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP455088.RA5ZhUjZTeWwHtYSF8sSDnWPYrWXqevTDEwJtu1Bre-eA130_assertion> ?p ?o ?g. }
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- NP455088.RA5ZhUjZTeWwHtYSF8sSDnWPYrWXqevTDEwJtu1Bre-eA130_assertion type Assertion NP455088.RA5ZhUjZTeWwHtYSF8sSDnWPYrWXqevTDEwJtu1Bre-eA130_head.
- NP455088.RA5ZhUjZTeWwHtYSF8sSDnWPYrWXqevTDEwJtu1Bre-eA130_assertion description "[It is a heritable disorder characterised by defective mineralisation of the skeletal and dental structures of the body and a deficiency in the liver/bone/kidney (L/B/K) isoenzyme of alkaline phosphatase (ALP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP455088.RA5ZhUjZTeWwHtYSF8sSDnWPYrWXqevTDEwJtu1Bre-eA130_provenance.
- NP455088.RA5ZhUjZTeWwHtYSF8sSDnWPYrWXqevTDEwJtu1Bre-eA130_assertion evidence source_evidence_literature NP455088.RA5ZhUjZTeWwHtYSF8sSDnWPYrWXqevTDEwJtu1Bre-eA130_provenance.
- NP455088.RA5ZhUjZTeWwHtYSF8sSDnWPYrWXqevTDEwJtu1Bre-eA130_assertion SIO_000772 8227447 NP455088.RA5ZhUjZTeWwHtYSF8sSDnWPYrWXqevTDEwJtu1Bre-eA130_provenance.
- NP455088.RA5ZhUjZTeWwHtYSF8sSDnWPYrWXqevTDEwJtu1Bre-eA130_assertion wasDerivedFrom befree-20140225 NP455088.RA5ZhUjZTeWwHtYSF8sSDnWPYrWXqevTDEwJtu1Bre-eA130_provenance.
- NP455088.RA5ZhUjZTeWwHtYSF8sSDnWPYrWXqevTDEwJtu1Bre-eA130_assertion wasGeneratedBy ECO_0000203 NP455088.RA5ZhUjZTeWwHtYSF8sSDnWPYrWXqevTDEwJtu1Bre-eA130_provenance.