Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP479296.RAQ7uvC08Y9LIxLWe_b_E5tGGKCcM6Rh4jP1NCDfywn6I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP479296.RAQ7uvC08Y9LIxLWe_b_E5tGGKCcM6Rh4jP1NCDfywn6I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP479296.RAQ7uvC08Y9LIxLWe_b_E5tGGKCcM6Rh4jP1NCDfywn6I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP479296.RAQ7uvC08Y9LIxLWe_b_E5tGGKCcM6Rh4jP1NCDfywn6I130_provenance.
- NP479296.RAQ7uvC08Y9LIxLWe_b_E5tGGKCcM6Rh4jP1NCDfywn6I130_assertion description "[Mutation analyses for SCA1, 2, 3, 6, 7, 8, 10, 12, 17, and DRPLA and frataxin genes were performed for 251 unrelated Finnish patients who presented with progressive ataxia disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP479296.RAQ7uvC08Y9LIxLWe_b_E5tGGKCcM6Rh4jP1NCDfywn6I130_provenance.
- NP479296.RAQ7uvC08Y9LIxLWe_b_E5tGGKCcM6Rh4jP1NCDfywn6I130_assertion evidence source_evidence_literature NP479296.RAQ7uvC08Y9LIxLWe_b_E5tGGKCcM6Rh4jP1NCDfywn6I130_provenance.
- NP479296.RAQ7uvC08Y9LIxLWe_b_E5tGGKCcM6Rh4jP1NCDfywn6I130_assertion SIO_000772 15691283 NP479296.RAQ7uvC08Y9LIxLWe_b_E5tGGKCcM6Rh4jP1NCDfywn6I130_provenance.
- NP479296.RAQ7uvC08Y9LIxLWe_b_E5tGGKCcM6Rh4jP1NCDfywn6I130_assertion wasDerivedFrom befree-2016 NP479296.RAQ7uvC08Y9LIxLWe_b_E5tGGKCcM6Rh4jP1NCDfywn6I130_provenance.
- NP479296.RAQ7uvC08Y9LIxLWe_b_E5tGGKCcM6Rh4jP1NCDfywn6I130_assertion wasGeneratedBy ECO_0000203 NP479296.RAQ7uvC08Y9LIxLWe_b_E5tGGKCcM6Rh4jP1NCDfywn6I130_provenance.
- befree-2016 importedOn "2016-02-19" NP479296.RAQ7uvC08Y9LIxLWe_b_E5tGGKCcM6Rh4jP1NCDfywn6I130_provenance.