Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1098.RA5C4SEfOJZgxAuW3fuhBKWPPH8KcNtoM8VJVtPqRpIkk130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1098.RA5C4SEfOJZgxAuW3fuhBKWPPH8KcNtoM8VJVtPqRpIkk130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1098.RA5C4SEfOJZgxAuW3fuhBKWPPH8KcNtoM8VJVtPqRpIkk130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1098.RA5C4SEfOJZgxAuW3fuhBKWPPH8KcNtoM8VJVtPqRpIkk130_provenance.
- NP1098.RA5C4SEfOJZgxAuW3fuhBKWPPH8KcNtoM8VJVtPqRpIkk130_assertion description "[Hypophosphatasia is an inherited disorder characterized by defective bone mineralization and a deficiency of tissue-nonspecific alkaline phosphatase (TNSALP) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1098.RA5C4SEfOJZgxAuW3fuhBKWPPH8KcNtoM8VJVtPqRpIkk130_provenance.
- NP1098.RA5C4SEfOJZgxAuW3fuhBKWPPH8KcNtoM8VJVtPqRpIkk130_assertion evidence source_evidence_curated NP1098.RA5C4SEfOJZgxAuW3fuhBKWPPH8KcNtoM8VJVtPqRpIkk130_provenance.
- NP1098.RA5C4SEfOJZgxAuW3fuhBKWPPH8KcNtoM8VJVtPqRpIkk130_assertion SIO_000772 11479741 NP1098.RA5C4SEfOJZgxAuW3fuhBKWPPH8KcNtoM8VJVtPqRpIkk130_provenance.
- NP1098.RA5C4SEfOJZgxAuW3fuhBKWPPH8KcNtoM8VJVtPqRpIkk130_assertion wasDerivedFrom uniprot-20150221 NP1098.RA5C4SEfOJZgxAuW3fuhBKWPPH8KcNtoM8VJVtPqRpIkk130_provenance.
- NP1098.RA5C4SEfOJZgxAuW3fuhBKWPPH8KcNtoM8VJVtPqRpIkk130_assertion wasGeneratedBy ECO_0000218 NP1098.RA5C4SEfOJZgxAuW3fuhBKWPPH8KcNtoM8VJVtPqRpIkk130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP1098.RA5C4SEfOJZgxAuW3fuhBKWPPH8KcNtoM8VJVtPqRpIkk130_provenance.