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- source_evidence_literature type ECO_0000212 NP1345335.RADRaFBxNMO7ouJN98SFn61owLxU61XBK2x0_qgBUBb0U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1345335.RADRaFBxNMO7ouJN98SFn61owLxU61XBK2x0_qgBUBb0U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1345335.RADRaFBxNMO7ouJN98SFn61owLxU61XBK2x0_qgBUBb0U130_provenance.
- NP1345335.RADRaFBxNMO7ouJN98SFn61owLxU61XBK2x0_qgBUBb0U130_assertion description "[Identification of 13 new mutations in the vasopressin-neurophysin II gene in 17 kindreds with familial autosomal dominant neurohypophyseal diabetes insipidus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1345335.RADRaFBxNMO7ouJN98SFn61owLxU61XBK2x0_qgBUBb0U130_provenance.
- NP1345335.RADRaFBxNMO7ouJN98SFn61owLxU61XBK2x0_qgBUBb0U130_assertion evidence source_evidence_literature NP1345335.RADRaFBxNMO7ouJN98SFn61owLxU61XBK2x0_qgBUBb0U130_provenance.
- NP1345335.RADRaFBxNMO7ouJN98SFn61owLxU61XBK2x0_qgBUBb0U130_assertion SIO_000772 8554046 NP1345335.RADRaFBxNMO7ouJN98SFn61owLxU61XBK2x0_qgBUBb0U130_provenance.
- NP1345335.RADRaFBxNMO7ouJN98SFn61owLxU61XBK2x0_qgBUBb0U130_assertion wasDerivedFrom befree-2016 NP1345335.RADRaFBxNMO7ouJN98SFn61owLxU61XBK2x0_qgBUBb0U130_provenance.
- NP1345335.RADRaFBxNMO7ouJN98SFn61owLxU61XBK2x0_qgBUBb0U130_assertion wasGeneratedBy ECO_0000203 NP1345335.RADRaFBxNMO7ouJN98SFn61owLxU61XBK2x0_qgBUBb0U130_provenance.
- befree-2016 importedOn "2016-02-19" NP1345335.RADRaFBxNMO7ouJN98SFn61owLxU61XBK2x0_qgBUBb0U130_provenance.