Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_provenance.
- NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_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." NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_provenance.
- NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_assertion evidence source_evidence_literature NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_provenance.
- NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_assertion SIO_000772 20828673 NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_provenance.
- NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_assertion wasDerivedFrom befree-20140225 NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_provenance.
- NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_assertion wasGeneratedBy ECO_0000203 NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_provenance.