Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP215739.RAzmPnPEnGcnExrztJzB09FofKSpYlCQNUqkcVEKo1zUk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP215739.RAzmPnPEnGcnExrztJzB09FofKSpYlCQNUqkcVEKo1zUk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215739.RAzmPnPEnGcnExrztJzB09FofKSpYlCQNUqkcVEKo1zUk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215739.RAzmPnPEnGcnExrztJzB09FofKSpYlCQNUqkcVEKo1zUk130_provenance.
- NP215739.RAzmPnPEnGcnExrztJzB09FofKSpYlCQNUqkcVEKo1zUk130_assertion description "[Altogether, our findings support ATXN2 high-length repeats as a risk factor for ALS and further indicate a genetic link between spinocerebellar ataxia type 2 and ALS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215739.RAzmPnPEnGcnExrztJzB09FofKSpYlCQNUqkcVEKo1zUk130_provenance.
- NP215739.RAzmPnPEnGcnExrztJzB09FofKSpYlCQNUqkcVEKo1zUk130_assertion evidence source_evidence_literature NP215739.RAzmPnPEnGcnExrztJzB09FofKSpYlCQNUqkcVEKo1zUk130_provenance.
- NP215739.RAzmPnPEnGcnExrztJzB09FofKSpYlCQNUqkcVEKo1zUk130_assertion SIO_000772 21670397 NP215739.RAzmPnPEnGcnExrztJzB09FofKSpYlCQNUqkcVEKo1zUk130_provenance.
- NP215739.RAzmPnPEnGcnExrztJzB09FofKSpYlCQNUqkcVEKo1zUk130_assertion wasDerivedFrom befree-20140225 NP215739.RAzmPnPEnGcnExrztJzB09FofKSpYlCQNUqkcVEKo1zUk130_provenance.
- NP215739.RAzmPnPEnGcnExrztJzB09FofKSpYlCQNUqkcVEKo1zUk130_assertion wasGeneratedBy ECO_0000203 NP215739.RAzmPnPEnGcnExrztJzB09FofKSpYlCQNUqkcVEKo1zUk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP215739.RAzmPnPEnGcnExrztJzB09FofKSpYlCQNUqkcVEKo1zUk130_provenance.