Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP499905.RAC_jfMvz1xZymnUXbK65tgN5GbLG0R1LGiTKi999kU2Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP499905.RAC_jfMvz1xZymnUXbK65tgN5GbLG0R1LGiTKi999kU2Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499905.RAC_jfMvz1xZymnUXbK65tgN5GbLG0R1LGiTKi999kU2Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499905.RAC_jfMvz1xZymnUXbK65tgN5GbLG0R1LGiTKi999kU2Q130_provenance.
- NP499905.RAC_jfMvz1xZymnUXbK65tgN5GbLG0R1LGiTKi999kU2Q130_assertion description "[In gain-of-function CaSR mutations, the genetic abnormalities increase CaSR activity leading to the development of such clinical manifestations as hypercalciuric hypocalcemia and hypoparathyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499905.RAC_jfMvz1xZymnUXbK65tgN5GbLG0R1LGiTKi999kU2Q130_provenance.
- NP499905.RAC_jfMvz1xZymnUXbK65tgN5GbLG0R1LGiTKi999kU2Q130_assertion evidence source_evidence_literature NP499905.RAC_jfMvz1xZymnUXbK65tgN5GbLG0R1LGiTKi999kU2Q130_provenance.
- NP499905.RAC_jfMvz1xZymnUXbK65tgN5GbLG0R1LGiTKi999kU2Q130_assertion SIO_000772 15960151 NP499905.RAC_jfMvz1xZymnUXbK65tgN5GbLG0R1LGiTKi999kU2Q130_provenance.
- NP499905.RAC_jfMvz1xZymnUXbK65tgN5GbLG0R1LGiTKi999kU2Q130_assertion wasDerivedFrom befree-2016 NP499905.RAC_jfMvz1xZymnUXbK65tgN5GbLG0R1LGiTKi999kU2Q130_provenance.
- NP499905.RAC_jfMvz1xZymnUXbK65tgN5GbLG0R1LGiTKi999kU2Q130_assertion wasGeneratedBy ECO_0000203 NP499905.RAC_jfMvz1xZymnUXbK65tgN5GbLG0R1LGiTKi999kU2Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP499905.RAC_jfMvz1xZymnUXbK65tgN5GbLG0R1LGiTKi999kU2Q130_provenance.