Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP236870.RAgGpLslPpLCxcRr3hdV6Gl-Ws1HQEWEB_v7aq-P1kHqc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP236870.RAgGpLslPpLCxcRr3hdV6Gl-Ws1HQEWEB_v7aq-P1kHqc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP236870.RAgGpLslPpLCxcRr3hdV6Gl-Ws1HQEWEB_v7aq-P1kHqc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP236870.RAgGpLslPpLCxcRr3hdV6Gl-Ws1HQEWEB_v7aq-P1kHqc130_provenance.
- NP236870.RAgGpLslPpLCxcRr3hdV6Gl-Ws1HQEWEB_v7aq-P1kHqc130_assertion description "[Mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene cause hypophosphatasia (HPP), an inborn error of metabolism characterized by defects in bone and teeth mineralization accompanying subnormal levels of serum alkaline phosphatase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP236870.RAgGpLslPpLCxcRr3hdV6Gl-Ws1HQEWEB_v7aq-P1kHqc130_provenance.
- NP236870.RAgGpLslPpLCxcRr3hdV6Gl-Ws1HQEWEB_v7aq-P1kHqc130_assertion evidence source_evidence_literature NP236870.RAgGpLslPpLCxcRr3hdV6Gl-Ws1HQEWEB_v7aq-P1kHqc130_provenance.
- NP236870.RAgGpLslPpLCxcRr3hdV6Gl-Ws1HQEWEB_v7aq-P1kHqc130_assertion SIO_000772 23039266 NP236870.RAgGpLslPpLCxcRr3hdV6Gl-Ws1HQEWEB_v7aq-P1kHqc130_provenance.
- NP236870.RAgGpLslPpLCxcRr3hdV6Gl-Ws1HQEWEB_v7aq-P1kHqc130_assertion wasDerivedFrom befree-20150227 NP236870.RAgGpLslPpLCxcRr3hdV6Gl-Ws1HQEWEB_v7aq-P1kHqc130_provenance.
- NP236870.RAgGpLslPpLCxcRr3hdV6Gl-Ws1HQEWEB_v7aq-P1kHqc130_assertion wasGeneratedBy ECO_0000203 NP236870.RAgGpLslPpLCxcRr3hdV6Gl-Ws1HQEWEB_v7aq-P1kHqc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP236870.RAgGpLslPpLCxcRr3hdV6Gl-Ws1HQEWEB_v7aq-P1kHqc130_provenance.