Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP400058.RAtexrrlruri-tuwtC30s5gPavJmgu04wkMqBedMmcG8U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP400058.RAtexrrlruri-tuwtC30s5gPavJmgu04wkMqBedMmcG8U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400058.RAtexrrlruri-tuwtC30s5gPavJmgu04wkMqBedMmcG8U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400058.RAtexrrlruri-tuwtC30s5gPavJmgu04wkMqBedMmcG8U130_provenance.
- NP400058.RAtexrrlruri-tuwtC30s5gPavJmgu04wkMqBedMmcG8U130_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." NP400058.RAtexrrlruri-tuwtC30s5gPavJmgu04wkMqBedMmcG8U130_provenance.
- NP400058.RAtexrrlruri-tuwtC30s5gPavJmgu04wkMqBedMmcG8U130_assertion evidence source_evidence_literature NP400058.RAtexrrlruri-tuwtC30s5gPavJmgu04wkMqBedMmcG8U130_provenance.
- NP400058.RAtexrrlruri-tuwtC30s5gPavJmgu04wkMqBedMmcG8U130_assertion SIO_000772 20828673 NP400058.RAtexrrlruri-tuwtC30s5gPavJmgu04wkMqBedMmcG8U130_provenance.
- NP400058.RAtexrrlruri-tuwtC30s5gPavJmgu04wkMqBedMmcG8U130_assertion wasDerivedFrom befree-20140225 NP400058.RAtexrrlruri-tuwtC30s5gPavJmgu04wkMqBedMmcG8U130_provenance.
- NP400058.RAtexrrlruri-tuwtC30s5gPavJmgu04wkMqBedMmcG8U130_assertion wasGeneratedBy ECO_0000203 NP400058.RAtexrrlruri-tuwtC30s5gPavJmgu04wkMqBedMmcG8U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP400058.RAtexrrlruri-tuwtC30s5gPavJmgu04wkMqBedMmcG8U130_provenance.