Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1018372.RA38HDcsLog9E0Bk1z8LeXfG1QHlP2CMWQXjzYZvqZiCs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1018372.RA38HDcsLog9E0Bk1z8LeXfG1QHlP2CMWQXjzYZvqZiCs130_assertion type Assertion NP1018372.RA38HDcsLog9E0Bk1z8LeXfG1QHlP2CMWQXjzYZvqZiCs130_head.
- NP1018372.RA38HDcsLog9E0Bk1z8LeXfG1QHlP2CMWQXjzYZvqZiCs130_assertion description "[Mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene cause hypophosphatasia (HPP), an inborn error of metabolism characterized by defects in bone and teeth mineralization accompanying subnormal levels of serum alkaline phosphatase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1018372.RA38HDcsLog9E0Bk1z8LeXfG1QHlP2CMWQXjzYZvqZiCs130_provenance.
- NP1018372.RA38HDcsLog9E0Bk1z8LeXfG1QHlP2CMWQXjzYZvqZiCs130_assertion evidence source_evidence_literature NP1018372.RA38HDcsLog9E0Bk1z8LeXfG1QHlP2CMWQXjzYZvqZiCs130_provenance.
- NP1018372.RA38HDcsLog9E0Bk1z8LeXfG1QHlP2CMWQXjzYZvqZiCs130_assertion SIO_000772 23039266 NP1018372.RA38HDcsLog9E0Bk1z8LeXfG1QHlP2CMWQXjzYZvqZiCs130_provenance.
- NP1018372.RA38HDcsLog9E0Bk1z8LeXfG1QHlP2CMWQXjzYZvqZiCs130_assertion wasDerivedFrom befree-2016 NP1018372.RA38HDcsLog9E0Bk1z8LeXfG1QHlP2CMWQXjzYZvqZiCs130_provenance.
- NP1018372.RA38HDcsLog9E0Bk1z8LeXfG1QHlP2CMWQXjzYZvqZiCs130_assertion wasGeneratedBy ECO_0000203 NP1018372.RA38HDcsLog9E0Bk1z8LeXfG1QHlP2CMWQXjzYZvqZiCs130_provenance.