Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP566083.RA14Wd81Sh-y5uyfM9mgtSsUnJF6_Gfrsyzx4G-zKsLsw130_assertion> ?p ?o ?g. }
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- NP566083.RA14Wd81Sh-y5uyfM9mgtSsUnJF6_Gfrsyzx4G-zKsLsw130_assertion type Assertion NP566083.RA14Wd81Sh-y5uyfM9mgtSsUnJF6_Gfrsyzx4G-zKsLsw130_head.
- NP566083.RA14Wd81Sh-y5uyfM9mgtSsUnJF6_Gfrsyzx4G-zKsLsw130_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." NP566083.RA14Wd81Sh-y5uyfM9mgtSsUnJF6_Gfrsyzx4G-zKsLsw130_provenance.
- NP566083.RA14Wd81Sh-y5uyfM9mgtSsUnJF6_Gfrsyzx4G-zKsLsw130_assertion evidence source_evidence_literature NP566083.RA14Wd81Sh-y5uyfM9mgtSsUnJF6_Gfrsyzx4G-zKsLsw130_provenance.
- NP566083.RA14Wd81Sh-y5uyfM9mgtSsUnJF6_Gfrsyzx4G-zKsLsw130_assertion SIO_000772 10679946 NP566083.RA14Wd81Sh-y5uyfM9mgtSsUnJF6_Gfrsyzx4G-zKsLsw130_provenance.
- NP566083.RA14Wd81Sh-y5uyfM9mgtSsUnJF6_Gfrsyzx4G-zKsLsw130_assertion wasDerivedFrom befree-20140225 NP566083.RA14Wd81Sh-y5uyfM9mgtSsUnJF6_Gfrsyzx4G-zKsLsw130_provenance.
- NP566083.RA14Wd81Sh-y5uyfM9mgtSsUnJF6_Gfrsyzx4G-zKsLsw130_assertion wasGeneratedBy ECO_0000203 NP566083.RA14Wd81Sh-y5uyfM9mgtSsUnJF6_Gfrsyzx4G-zKsLsw130_provenance.