Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP512521.RAs6CaFsUorRTaW2rTG8kkcDHSUXUcs4UDB81jnAlYK_c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP512521.RAs6CaFsUorRTaW2rTG8kkcDHSUXUcs4UDB81jnAlYK_c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP512521.RAs6CaFsUorRTaW2rTG8kkcDHSUXUcs4UDB81jnAlYK_c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP512521.RAs6CaFsUorRTaW2rTG8kkcDHSUXUcs4UDB81jnAlYK_c130_provenance.
- NP512521.RAs6CaFsUorRTaW2rTG8kkcDHSUXUcs4UDB81jnAlYK_c130_assertion description "[We investigated the relative prevalence of SCA1-3, 6-8, 12, 17; dentate-rubro-pallidoluysian atrophy; and Friedreich's ataxia (FRDA) in Serbian patients with adult-onset (>20 years of age) hereditary and sporadic SCAs, and compared clinical features of patients with genetically confirmed SCAs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP512521.RAs6CaFsUorRTaW2rTG8kkcDHSUXUcs4UDB81jnAlYK_c130_provenance.
- NP512521.RAs6CaFsUorRTaW2rTG8kkcDHSUXUcs4UDB81jnAlYK_c130_assertion evidence source_evidence_literature NP512521.RAs6CaFsUorRTaW2rTG8kkcDHSUXUcs4UDB81jnAlYK_c130_provenance.
- NP512521.RAs6CaFsUorRTaW2rTG8kkcDHSUXUcs4UDB81jnAlYK_c130_assertion SIO_000772 16149098 NP512521.RAs6CaFsUorRTaW2rTG8kkcDHSUXUcs4UDB81jnAlYK_c130_provenance.
- NP512521.RAs6CaFsUorRTaW2rTG8kkcDHSUXUcs4UDB81jnAlYK_c130_assertion wasDerivedFrom befree-2016 NP512521.RAs6CaFsUorRTaW2rTG8kkcDHSUXUcs4UDB81jnAlYK_c130_provenance.
- NP512521.RAs6CaFsUorRTaW2rTG8kkcDHSUXUcs4UDB81jnAlYK_c130_assertion wasGeneratedBy ECO_0000203 NP512521.RAs6CaFsUorRTaW2rTG8kkcDHSUXUcs4UDB81jnAlYK_c130_provenance.
- befree-2016 importedOn "2016-02-19" NP512521.RAs6CaFsUorRTaW2rTG8kkcDHSUXUcs4UDB81jnAlYK_c130_provenance.