Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP853779.RACMSsVhDoVguwQw-n3mTkReIcrUd2nK_aIFXpllBXydk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP853779.RACMSsVhDoVguwQw-n3mTkReIcrUd2nK_aIFXpllBXydk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP853779.RACMSsVhDoVguwQw-n3mTkReIcrUd2nK_aIFXpllBXydk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP853779.RACMSsVhDoVguwQw-n3mTkReIcrUd2nK_aIFXpllBXydk130_provenance.
- NP853779.RACMSsVhDoVguwQw-n3mTkReIcrUd2nK_aIFXpllBXydk130_assertion description "[Hypophosphatasia (HPP) is an inherited disorder characterised by defective bone and tooth mineralisation and deficient serum and bone alkaline phosphatase activity, and it results from mutations in alkaline phosphatase (ALPL) encoding tissue-nonspecific alkaline phosphatase (TNAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853779.RACMSsVhDoVguwQw-n3mTkReIcrUd2nK_aIFXpllBXydk130_provenance.
- NP853779.RACMSsVhDoVguwQw-n3mTkReIcrUd2nK_aIFXpllBXydk130_assertion evidence source_evidence_literature NP853779.RACMSsVhDoVguwQw-n3mTkReIcrUd2nK_aIFXpllBXydk130_provenance.
- NP853779.RACMSsVhDoVguwQw-n3mTkReIcrUd2nK_aIFXpllBXydk130_assertion SIO_000772 20828673 NP853779.RACMSsVhDoVguwQw-n3mTkReIcrUd2nK_aIFXpllBXydk130_provenance.
- NP853779.RACMSsVhDoVguwQw-n3mTkReIcrUd2nK_aIFXpllBXydk130_assertion wasDerivedFrom befree-20140225 NP853779.RACMSsVhDoVguwQw-n3mTkReIcrUd2nK_aIFXpllBXydk130_provenance.
- NP853779.RACMSsVhDoVguwQw-n3mTkReIcrUd2nK_aIFXpllBXydk130_assertion wasGeneratedBy ECO_0000203 NP853779.RACMSsVhDoVguwQw-n3mTkReIcrUd2nK_aIFXpllBXydk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP853779.RACMSsVhDoVguwQw-n3mTkReIcrUd2nK_aIFXpllBXydk130_provenance.