Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP190.RACD-Dywj1K0chsnqdoJ1XJJgiDTyoGIpELh6Fc5CwBQc130_assertion> ?p ?o ?g. }
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- NP190.RACD-Dywj1K0chsnqdoJ1XJJgiDTyoGIpELh6Fc5CwBQc130_assertion type Assertion NP190.RACD-Dywj1K0chsnqdoJ1XJJgiDTyoGIpELh6Fc5CwBQc130_head.
- NP190.RACD-Dywj1K0chsnqdoJ1XJJgiDTyoGIpELh6Fc5CwBQc130_assertion wasGeneratedBy ECO_0000218 NP190.RACD-Dywj1K0chsnqdoJ1XJJgiDTyoGIpELh6Fc5CwBQc130_provenance.
- NP190.RACD-Dywj1K0chsnqdoJ1XJJgiDTyoGIpELh6Fc5CwBQc130_assertion wasDerivedFrom uniprot-2016 NP190.RACD-Dywj1K0chsnqdoJ1XJJgiDTyoGIpELh6Fc5CwBQc130_provenance.
- NP190.RACD-Dywj1K0chsnqdoJ1XJJgiDTyoGIpELh6Fc5CwBQc130_assertion SIO_000772 10332035 NP190.RACD-Dywj1K0chsnqdoJ1XJJgiDTyoGIpELh6Fc5CwBQc130_provenance.
- NP190.RACD-Dywj1K0chsnqdoJ1XJJgiDTyoGIpELh6Fc5CwBQc130_assertion evidence source_evidence_curated NP190.RACD-Dywj1K0chsnqdoJ1XJJgiDTyoGIpELh6Fc5CwBQc130_provenance.
- NP190.RACD-Dywj1K0chsnqdoJ1XJJgiDTyoGIpELh6Fc5CwBQc130_assertion description "[They also confirm that the extremely high phenotypic heterogeneity observed in patients with hypophosphatasia was due mainly to variable residual enzymatic activities allowed by missense mutations found in the human TNSALP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP190.RACD-Dywj1K0chsnqdoJ1XJJgiDTyoGIpELh6Fc5CwBQc130_provenance.