Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP507784.RAIrFQLTCzlSHBBZox3MNtugL9OzcgsBHzoWqA5LnUOmo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP507784.RAIrFQLTCzlSHBBZox3MNtugL9OzcgsBHzoWqA5LnUOmo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP507784.RAIrFQLTCzlSHBBZox3MNtugL9OzcgsBHzoWqA5LnUOmo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP507784.RAIrFQLTCzlSHBBZox3MNtugL9OzcgsBHzoWqA5LnUOmo130_provenance.
- befree-2016 importedOn "2016-02-19" NP507784.RAIrFQLTCzlSHBBZox3MNtugL9OzcgsBHzoWqA5LnUOmo130_provenance.
- NP507784.RAIrFQLTCzlSHBBZox3MNtugL9OzcgsBHzoWqA5LnUOmo130_assertion wasGeneratedBy ECO_0000203 NP507784.RAIrFQLTCzlSHBBZox3MNtugL9OzcgsBHzoWqA5LnUOmo130_provenance.
- NP507784.RAIrFQLTCzlSHBBZox3MNtugL9OzcgsBHzoWqA5LnUOmo130_assertion wasDerivedFrom befree-2016 NP507784.RAIrFQLTCzlSHBBZox3MNtugL9OzcgsBHzoWqA5LnUOmo130_provenance.
- NP507784.RAIrFQLTCzlSHBBZox3MNtugL9OzcgsBHzoWqA5LnUOmo130_assertion SIO_000772 16085057 NP507784.RAIrFQLTCzlSHBBZox3MNtugL9OzcgsBHzoWqA5LnUOmo130_provenance.
- NP507784.RAIrFQLTCzlSHBBZox3MNtugL9OzcgsBHzoWqA5LnUOmo130_assertion evidence source_evidence_literature NP507784.RAIrFQLTCzlSHBBZox3MNtugL9OzcgsBHzoWqA5LnUOmo130_provenance.
- NP507784.RAIrFQLTCzlSHBBZox3MNtugL9OzcgsBHzoWqA5LnUOmo130_assertion description "[Mutations in the ALS2 gene has recently been linked to cases of juvenile amyotrophic lateral sclerosis, juvenile primary lateral sclerosis and ascending hereditary spastic paralysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP507784.RAIrFQLTCzlSHBBZox3MNtugL9OzcgsBHzoWqA5LnUOmo130_provenance.