Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP236926.RAkhDbVTh02HhYzBhfEb0dzQH--5rhQJuj7P1sKJe6CAY130_assertion> ?p ?o ?g. }
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- NP236926.RAkhDbVTh02HhYzBhfEb0dzQH--5rhQJuj7P1sKJe6CAY130_assertion type Assertion NP236926.RAkhDbVTh02HhYzBhfEb0dzQH--5rhQJuj7P1sKJe6CAY130_head.
- NP236926.RAkhDbVTh02HhYzBhfEb0dzQH--5rhQJuj7P1sKJe6CAY130_assertion description "[Hypophosphatasia is a rare inherited disorder characterized by defective bone mineralization and deficiency of serum and liver/bone/kidney-type alkaline phosphatase (L/B/K ALP) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP236926.RAkhDbVTh02HhYzBhfEb0dzQH--5rhQJuj7P1sKJe6CAY130_provenance.
- NP236926.RAkhDbVTh02HhYzBhfEb0dzQH--5rhQJuj7P1sKJe6CAY130_assertion evidence source_evidence_literature NP236926.RAkhDbVTh02HhYzBhfEb0dzQH--5rhQJuj7P1sKJe6CAY130_provenance.
- NP236926.RAkhDbVTh02HhYzBhfEb0dzQH--5rhQJuj7P1sKJe6CAY130_assertion SIO_000772 10679946 NP236926.RAkhDbVTh02HhYzBhfEb0dzQH--5rhQJuj7P1sKJe6CAY130_provenance.
- NP236926.RAkhDbVTh02HhYzBhfEb0dzQH--5rhQJuj7P1sKJe6CAY130_assertion wasDerivedFrom befree-20150227 NP236926.RAkhDbVTh02HhYzBhfEb0dzQH--5rhQJuj7P1sKJe6CAY130_provenance.
- NP236926.RAkhDbVTh02HhYzBhfEb0dzQH--5rhQJuj7P1sKJe6CAY130_assertion wasGeneratedBy ECO_0000203 NP236926.RAkhDbVTh02HhYzBhfEb0dzQH--5rhQJuj7P1sKJe6CAY130_provenance.