Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1182911.RA64ULb7FLrPhnB5O4VuLc75TZ-y4QYd7NV3L32JCwy2A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1182911.RA64ULb7FLrPhnB5O4VuLc75TZ-y4QYd7NV3L32JCwy2A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1182911.RA64ULb7FLrPhnB5O4VuLc75TZ-y4QYd7NV3L32JCwy2A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1182911.RA64ULb7FLrPhnB5O4VuLc75TZ-y4QYd7NV3L32JCwy2A130_provenance.
- NP1182911.RA64ULb7FLrPhnB5O4VuLc75TZ-y4QYd7NV3L32JCwy2A130_assertion description "[Subjects with SPG35 had intellectual impairment, spastic paraplegia, thin corpus callosum, white matter hyperintensities, and cerebellar atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1182911.RA64ULb7FLrPhnB5O4VuLc75TZ-y4QYd7NV3L32JCwy2A130_provenance.
- NP1182911.RA64ULb7FLrPhnB5O4VuLc75TZ-y4QYd7NV3L32JCwy2A130_assertion evidence source_evidence_literature NP1182911.RA64ULb7FLrPhnB5O4VuLc75TZ-y4QYd7NV3L32JCwy2A130_provenance.
- NP1182911.RA64ULb7FLrPhnB5O4VuLc75TZ-y4QYd7NV3L32JCwy2A130_assertion SIO_000772 24833714 NP1182911.RA64ULb7FLrPhnB5O4VuLc75TZ-y4QYd7NV3L32JCwy2A130_provenance.
- NP1182911.RA64ULb7FLrPhnB5O4VuLc75TZ-y4QYd7NV3L32JCwy2A130_assertion wasDerivedFrom befree-2016 NP1182911.RA64ULb7FLrPhnB5O4VuLc75TZ-y4QYd7NV3L32JCwy2A130_provenance.
- NP1182911.RA64ULb7FLrPhnB5O4VuLc75TZ-y4QYd7NV3L32JCwy2A130_assertion wasGeneratedBy ECO_0000203 NP1182911.RA64ULb7FLrPhnB5O4VuLc75TZ-y4QYd7NV3L32JCwy2A130_provenance.
- befree-2016 importedOn "2016-02-19" NP1182911.RA64ULb7FLrPhnB5O4VuLc75TZ-y4QYd7NV3L32JCwy2A130_provenance.