Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP899919.RAzC4URbLeh_ZUtPxwSUrtItkgOY_uYefa3S7EzqRgT5M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP899919.RAzC4URbLeh_ZUtPxwSUrtItkgOY_uYefa3S7EzqRgT5M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP899919.RAzC4URbLeh_ZUtPxwSUrtItkgOY_uYefa3S7EzqRgT5M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP899919.RAzC4URbLeh_ZUtPxwSUrtItkgOY_uYefa3S7EzqRgT5M130_provenance.
- NP899919.RAzC4URbLeh_ZUtPxwSUrtItkgOY_uYefa3S7EzqRgT5M130_assertion description "[Hypophosphatasia is a heritable disorder characterized by defective bone mineralization and a deficiency of liver/bone/kidney alkaline phosphatase (L/B/K ALP) activity in serum and tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP899919.RAzC4URbLeh_ZUtPxwSUrtItkgOY_uYefa3S7EzqRgT5M130_provenance.
- NP899919.RAzC4URbLeh_ZUtPxwSUrtItkgOY_uYefa3S7EzqRgT5M130_assertion evidence source_evidence_literature NP899919.RAzC4URbLeh_ZUtPxwSUrtItkgOY_uYefa3S7EzqRgT5M130_provenance.
- NP899919.RAzC4URbLeh_ZUtPxwSUrtItkgOY_uYefa3S7EzqRgT5M130_assertion SIO_000772 2705456 NP899919.RAzC4URbLeh_ZUtPxwSUrtItkgOY_uYefa3S7EzqRgT5M130_provenance.
- NP899919.RAzC4URbLeh_ZUtPxwSUrtItkgOY_uYefa3S7EzqRgT5M130_assertion wasDerivedFrom befree-20140225 NP899919.RAzC4URbLeh_ZUtPxwSUrtItkgOY_uYefa3S7EzqRgT5M130_provenance.
- NP899919.RAzC4URbLeh_ZUtPxwSUrtItkgOY_uYefa3S7EzqRgT5M130_assertion wasGeneratedBy ECO_0000203 NP899919.RAzC4URbLeh_ZUtPxwSUrtItkgOY_uYefa3S7EzqRgT5M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP899919.RAzC4URbLeh_ZUtPxwSUrtItkgOY_uYefa3S7EzqRgT5M130_provenance.