Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP339822.RAzKvUhMn4XmwIwoOUSvko0bSgHc8a-X5s8GAOZFzVCMs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP339822.RAzKvUhMn4XmwIwoOUSvko0bSgHc8a-X5s8GAOZFzVCMs130_assertion type Assertion NP339822.RAzKvUhMn4XmwIwoOUSvko0bSgHc8a-X5s8GAOZFzVCMs130_head.
- NP339822.RAzKvUhMn4XmwIwoOUSvko0bSgHc8a-X5s8GAOZFzVCMs130_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." NP339822.RAzKvUhMn4XmwIwoOUSvko0bSgHc8a-X5s8GAOZFzVCMs130_provenance.
- NP339822.RAzKvUhMn4XmwIwoOUSvko0bSgHc8a-X5s8GAOZFzVCMs130_assertion evidence source_evidence_literature NP339822.RAzKvUhMn4XmwIwoOUSvko0bSgHc8a-X5s8GAOZFzVCMs130_provenance.
- NP339822.RAzKvUhMn4XmwIwoOUSvko0bSgHc8a-X5s8GAOZFzVCMs130_assertion SIO_000772 11438998 NP339822.RAzKvUhMn4XmwIwoOUSvko0bSgHc8a-X5s8GAOZFzVCMs130_provenance.
- NP339822.RAzKvUhMn4XmwIwoOUSvko0bSgHc8a-X5s8GAOZFzVCMs130_assertion wasDerivedFrom befree-20140225 NP339822.RAzKvUhMn4XmwIwoOUSvko0bSgHc8a-X5s8GAOZFzVCMs130_provenance.
- NP339822.RAzKvUhMn4XmwIwoOUSvko0bSgHc8a-X5s8GAOZFzVCMs130_assertion wasGeneratedBy ECO_0000203 NP339822.RAzKvUhMn4XmwIwoOUSvko0bSgHc8a-X5s8GAOZFzVCMs130_provenance.