Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP527769.RAPrhJrUtRdJ7SFNLmSOzwHCvmSQ1X-rcrwCga5urqBUM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP527769.RAPrhJrUtRdJ7SFNLmSOzwHCvmSQ1X-rcrwCga5urqBUM130_assertion type Assertion NP527769.RAPrhJrUtRdJ7SFNLmSOzwHCvmSQ1X-rcrwCga5urqBUM130_head.
- NP527769.RAPrhJrUtRdJ7SFNLmSOzwHCvmSQ1X-rcrwCga5urqBUM130_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." NP527769.RAPrhJrUtRdJ7SFNLmSOzwHCvmSQ1X-rcrwCga5urqBUM130_provenance.
- NP527769.RAPrhJrUtRdJ7SFNLmSOzwHCvmSQ1X-rcrwCga5urqBUM130_assertion evidence source_evidence_literature NP527769.RAPrhJrUtRdJ7SFNLmSOzwHCvmSQ1X-rcrwCga5urqBUM130_provenance.
- NP527769.RAPrhJrUtRdJ7SFNLmSOzwHCvmSQ1X-rcrwCga5urqBUM130_assertion SIO_000772 11438998 NP527769.RAPrhJrUtRdJ7SFNLmSOzwHCvmSQ1X-rcrwCga5urqBUM130_provenance.
- NP527769.RAPrhJrUtRdJ7SFNLmSOzwHCvmSQ1X-rcrwCga5urqBUM130_assertion wasDerivedFrom befree-20140225 NP527769.RAPrhJrUtRdJ7SFNLmSOzwHCvmSQ1X-rcrwCga5urqBUM130_provenance.
- NP527769.RAPrhJrUtRdJ7SFNLmSOzwHCvmSQ1X-rcrwCga5urqBUM130_assertion wasGeneratedBy ECO_0000203 NP527769.RAPrhJrUtRdJ7SFNLmSOzwHCvmSQ1X-rcrwCga5urqBUM130_provenance.