Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_provenance.
- NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_assertion description "[Two brothers with no copy of Cx32, 27 and 25 years old, showed steppage gait, moderate muscle atrophy and weakness, and mild sensory disturbance in the distal parts of the legs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_provenance.
- NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_assertion evidence source_evidence_literature NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_provenance.
- NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_assertion SIO_000772 11266688 NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_provenance.
- NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_assertion wasDerivedFrom befree-20150227 NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_provenance.
- NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_assertion wasGeneratedBy ECO_0000203 NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_provenance.