Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP577598.RA-kY_lrOLMSubP929r7ftOz4L4YwiEkm0Di84qGTyVS8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP577598.RA-kY_lrOLMSubP929r7ftOz4L4YwiEkm0Di84qGTyVS8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP577598.RA-kY_lrOLMSubP929r7ftOz4L4YwiEkm0Di84qGTyVS8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP577598.RA-kY_lrOLMSubP929r7ftOz4L4YwiEkm0Di84qGTyVS8130_provenance.
- NP577598.RA-kY_lrOLMSubP929r7ftOz4L4YwiEkm0Di84qGTyVS8130_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." NP577598.RA-kY_lrOLMSubP929r7ftOz4L4YwiEkm0Di84qGTyVS8130_provenance.
- NP577598.RA-kY_lrOLMSubP929r7ftOz4L4YwiEkm0Di84qGTyVS8130_assertion evidence source_evidence_literature NP577598.RA-kY_lrOLMSubP929r7ftOz4L4YwiEkm0Di84qGTyVS8130_provenance.
- NP577598.RA-kY_lrOLMSubP929r7ftOz4L4YwiEkm0Di84qGTyVS8130_assertion SIO_000772 20828673 NP577598.RA-kY_lrOLMSubP929r7ftOz4L4YwiEkm0Di84qGTyVS8130_provenance.
- NP577598.RA-kY_lrOLMSubP929r7ftOz4L4YwiEkm0Di84qGTyVS8130_assertion wasDerivedFrom befree-20140225 NP577598.RA-kY_lrOLMSubP929r7ftOz4L4YwiEkm0Di84qGTyVS8130_provenance.
- NP577598.RA-kY_lrOLMSubP929r7ftOz4L4YwiEkm0Di84qGTyVS8130_assertion wasGeneratedBy ECO_0000203 NP577598.RA-kY_lrOLMSubP929r7ftOz4L4YwiEkm0Di84qGTyVS8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP577598.RA-kY_lrOLMSubP929r7ftOz4L4YwiEkm0Di84qGTyVS8130_provenance.