Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615130.RAQXH0ea6Np3DfVxBH51vUbCczgeYNpWaNojulEQm_AcU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615130.RAQXH0ea6Np3DfVxBH51vUbCczgeYNpWaNojulEQm_AcU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615130.RAQXH0ea6Np3DfVxBH51vUbCczgeYNpWaNojulEQm_AcU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615130.RAQXH0ea6Np3DfVxBH51vUbCczgeYNpWaNojulEQm_AcU130_provenance.
- NP615130.RAQXH0ea6Np3DfVxBH51vUbCczgeYNpWaNojulEQm_AcU130_assertion description "[It is a heritable disorder characterised by defective mineralisation of the skeletal and dental structures of the body and a deficiency in the liver/bone/kidney (L/B/K) isoenzyme of alkaline phosphatase (ALP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615130.RAQXH0ea6Np3DfVxBH51vUbCczgeYNpWaNojulEQm_AcU130_provenance.
- NP615130.RAQXH0ea6Np3DfVxBH51vUbCczgeYNpWaNojulEQm_AcU130_assertion evidence source_evidence_literature NP615130.RAQXH0ea6Np3DfVxBH51vUbCczgeYNpWaNojulEQm_AcU130_provenance.
- NP615130.RAQXH0ea6Np3DfVxBH51vUbCczgeYNpWaNojulEQm_AcU130_assertion SIO_000772 8227447 NP615130.RAQXH0ea6Np3DfVxBH51vUbCczgeYNpWaNojulEQm_AcU130_provenance.
- NP615130.RAQXH0ea6Np3DfVxBH51vUbCczgeYNpWaNojulEQm_AcU130_assertion wasDerivedFrom befree-20140225 NP615130.RAQXH0ea6Np3DfVxBH51vUbCczgeYNpWaNojulEQm_AcU130_provenance.
- NP615130.RAQXH0ea6Np3DfVxBH51vUbCczgeYNpWaNojulEQm_AcU130_assertion wasGeneratedBy ECO_0000203 NP615130.RAQXH0ea6Np3DfVxBH51vUbCczgeYNpWaNojulEQm_AcU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615130.RAQXH0ea6Np3DfVxBH51vUbCczgeYNpWaNojulEQm_AcU130_provenance.