Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP430324.RAyzFvmGVrPZACgL7fd_cqZVy7XPwh5fVjzKIhmiOzbHU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP430324.RAyzFvmGVrPZACgL7fd_cqZVy7XPwh5fVjzKIhmiOzbHU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP430324.RAyzFvmGVrPZACgL7fd_cqZVy7XPwh5fVjzKIhmiOzbHU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP430324.RAyzFvmGVrPZACgL7fd_cqZVy7XPwh5fVjzKIhmiOzbHU130_provenance.
- NP430324.RAyzFvmGVrPZACgL7fd_cqZVy7XPwh5fVjzKIhmiOzbHU130_assertion description "[MJD/SCA3 (46%) was the most common autosomal dominant SCA in the Taiwanese cohort, followed by SCA6 (18%) and SCA1 (3%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430324.RAyzFvmGVrPZACgL7fd_cqZVy7XPwh5fVjzKIhmiOzbHU130_provenance.
- NP430324.RAyzFvmGVrPZACgL7fd_cqZVy7XPwh5fVjzKIhmiOzbHU130_assertion evidence source_evidence_literature NP430324.RAyzFvmGVrPZACgL7fd_cqZVy7XPwh5fVjzKIhmiOzbHU130_provenance.
- NP430324.RAyzFvmGVrPZACgL7fd_cqZVy7XPwh5fVjzKIhmiOzbHU130_assertion SIO_000772 14756671 NP430324.RAyzFvmGVrPZACgL7fd_cqZVy7XPwh5fVjzKIhmiOzbHU130_provenance.
- NP430324.RAyzFvmGVrPZACgL7fd_cqZVy7XPwh5fVjzKIhmiOzbHU130_assertion wasDerivedFrom befree-2016 NP430324.RAyzFvmGVrPZACgL7fd_cqZVy7XPwh5fVjzKIhmiOzbHU130_provenance.
- NP430324.RAyzFvmGVrPZACgL7fd_cqZVy7XPwh5fVjzKIhmiOzbHU130_assertion wasGeneratedBy ECO_0000203 NP430324.RAyzFvmGVrPZACgL7fd_cqZVy7XPwh5fVjzKIhmiOzbHU130_provenance.
- befree-2016 importedOn "2016-02-19" NP430324.RAyzFvmGVrPZACgL7fd_cqZVy7XPwh5fVjzKIhmiOzbHU130_provenance.