Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP275501.RAU5KX9FGLbQu61sTsrhODvkZACYq72Ko7jY1qK1M4k-c130_assertion> ?p ?o ?g. }
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- NP275501.RAU5KX9FGLbQu61sTsrhODvkZACYq72Ko7jY1qK1M4k-c130_assertion type Assertion NP275501.RAU5KX9FGLbQu61sTsrhODvkZACYq72Ko7jY1qK1M4k-c130_head.
- NP275501.RAU5KX9FGLbQu61sTsrhODvkZACYq72Ko7jY1qK1M4k-c130_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." NP275501.RAU5KX9FGLbQu61sTsrhODvkZACYq72Ko7jY1qK1M4k-c130_provenance.
- NP275501.RAU5KX9FGLbQu61sTsrhODvkZACYq72Ko7jY1qK1M4k-c130_assertion evidence source_evidence_literature NP275501.RAU5KX9FGLbQu61sTsrhODvkZACYq72Ko7jY1qK1M4k-c130_provenance.
- NP275501.RAU5KX9FGLbQu61sTsrhODvkZACYq72Ko7jY1qK1M4k-c130_assertion SIO_000772 10679946 NP275501.RAU5KX9FGLbQu61sTsrhODvkZACYq72Ko7jY1qK1M4k-c130_provenance.
- NP275501.RAU5KX9FGLbQu61sTsrhODvkZACYq72Ko7jY1qK1M4k-c130_assertion wasDerivedFrom befree-2016 NP275501.RAU5KX9FGLbQu61sTsrhODvkZACYq72Ko7jY1qK1M4k-c130_provenance.
- NP275501.RAU5KX9FGLbQu61sTsrhODvkZACYq72Ko7jY1qK1M4k-c130_assertion wasGeneratedBy ECO_0000203 NP275501.RAU5KX9FGLbQu61sTsrhODvkZACYq72Ko7jY1qK1M4k-c130_provenance.