Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_assertion> ?p ?o ?g. }
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- NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_assertion type Assertion NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_head.
- NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_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." NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_provenance.
- NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_assertion evidence source_evidence_literature NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_provenance.
- NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_assertion SIO_000772 10679946 NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_provenance.
- NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_assertion wasDerivedFrom befree-2016 NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_provenance.
- NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_assertion wasGeneratedBy ECO_0000203 NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_provenance.