Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP636838.RAUNWijjoRSmODjPJUoldA3UINYiermN-LT8Ccr6_KEKs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP636838.RAUNWijjoRSmODjPJUoldA3UINYiermN-LT8Ccr6_KEKs130_assertion type Assertion NP636838.RAUNWijjoRSmODjPJUoldA3UINYiermN-LT8Ccr6_KEKs130_head.
- NP636838.RAUNWijjoRSmODjPJUoldA3UINYiermN-LT8Ccr6_KEKs130_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." NP636838.RAUNWijjoRSmODjPJUoldA3UINYiermN-LT8Ccr6_KEKs130_provenance.
- NP636838.RAUNWijjoRSmODjPJUoldA3UINYiermN-LT8Ccr6_KEKs130_assertion evidence source_evidence_literature NP636838.RAUNWijjoRSmODjPJUoldA3UINYiermN-LT8Ccr6_KEKs130_provenance.
- NP636838.RAUNWijjoRSmODjPJUoldA3UINYiermN-LT8Ccr6_KEKs130_assertion SIO_000772 11438998 NP636838.RAUNWijjoRSmODjPJUoldA3UINYiermN-LT8Ccr6_KEKs130_provenance.
- NP636838.RAUNWijjoRSmODjPJUoldA3UINYiermN-LT8Ccr6_KEKs130_assertion wasDerivedFrom befree-20140225 NP636838.RAUNWijjoRSmODjPJUoldA3UINYiermN-LT8Ccr6_KEKs130_provenance.
- NP636838.RAUNWijjoRSmODjPJUoldA3UINYiermN-LT8Ccr6_KEKs130_assertion wasGeneratedBy ECO_0000203 NP636838.RAUNWijjoRSmODjPJUoldA3UINYiermN-LT8Ccr6_KEKs130_provenance.