Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP391247.RA2Fk0SSIButzqI7JdoZp6XMGOtNo0QN1_gVH8fvDHwg8130_assertion> ?p ?o ?g. }
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- NP391247.RA2Fk0SSIButzqI7JdoZp6XMGOtNo0QN1_gVH8fvDHwg8130_assertion type Assertion NP391247.RA2Fk0SSIButzqI7JdoZp6XMGOtNo0QN1_gVH8fvDHwg8130_head.
- NP391247.RA2Fk0SSIButzqI7JdoZp6XMGOtNo0QN1_gVH8fvDHwg8130_assertion description "[Hypophosphatasia is a rare inherited disorder characterized by defective bone mineralization and deficiency of serum and tissue liver/bone/kidney tissue alkaline phosphatase (L/B/K ALP) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391247.RA2Fk0SSIButzqI7JdoZp6XMGOtNo0QN1_gVH8fvDHwg8130_provenance.
- NP391247.RA2Fk0SSIButzqI7JdoZp6XMGOtNo0QN1_gVH8fvDHwg8130_assertion evidence source_evidence_literature NP391247.RA2Fk0SSIButzqI7JdoZp6XMGOtNo0QN1_gVH8fvDHwg8130_provenance.
- NP391247.RA2Fk0SSIButzqI7JdoZp6XMGOtNo0QN1_gVH8fvDHwg8130_assertion SIO_000772 11438998 NP391247.RA2Fk0SSIButzqI7JdoZp6XMGOtNo0QN1_gVH8fvDHwg8130_provenance.
- NP391247.RA2Fk0SSIButzqI7JdoZp6XMGOtNo0QN1_gVH8fvDHwg8130_assertion wasDerivedFrom befree-20140225 NP391247.RA2Fk0SSIButzqI7JdoZp6XMGOtNo0QN1_gVH8fvDHwg8130_provenance.
- NP391247.RA2Fk0SSIButzqI7JdoZp6XMGOtNo0QN1_gVH8fvDHwg8130_assertion wasGeneratedBy ECO_0000203 NP391247.RA2Fk0SSIButzqI7JdoZp6XMGOtNo0QN1_gVH8fvDHwg8130_provenance.