Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP887828.RAUfUwm-CCI4lh6dgyeplrG8gic80_91naCskKTRnnN7M130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP887828.RAUfUwm-CCI4lh6dgyeplrG8gic80_91naCskKTRnnN7M130_assertion type Assertion NP887828.RAUfUwm-CCI4lh6dgyeplrG8gic80_91naCskKTRnnN7M130_head.
- NP887828.RAUfUwm-CCI4lh6dgyeplrG8gic80_91naCskKTRnnN7M130_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." NP887828.RAUfUwm-CCI4lh6dgyeplrG8gic80_91naCskKTRnnN7M130_provenance.
- NP887828.RAUfUwm-CCI4lh6dgyeplrG8gic80_91naCskKTRnnN7M130_assertion evidence source_evidence_literature NP887828.RAUfUwm-CCI4lh6dgyeplrG8gic80_91naCskKTRnnN7M130_provenance.
- NP887828.RAUfUwm-CCI4lh6dgyeplrG8gic80_91naCskKTRnnN7M130_assertion SIO_000772 10679946 NP887828.RAUfUwm-CCI4lh6dgyeplrG8gic80_91naCskKTRnnN7M130_provenance.
- NP887828.RAUfUwm-CCI4lh6dgyeplrG8gic80_91naCskKTRnnN7M130_assertion wasDerivedFrom befree-20150227 NP887828.RAUfUwm-CCI4lh6dgyeplrG8gic80_91naCskKTRnnN7M130_provenance.
- NP887828.RAUfUwm-CCI4lh6dgyeplrG8gic80_91naCskKTRnnN7M130_assertion wasGeneratedBy ECO_0000203 NP887828.RAUfUwm-CCI4lh6dgyeplrG8gic80_91naCskKTRnnN7M130_provenance.