Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP794392.RAZSByKIZuOKi7aU3_l_AjMVxKYh92gEn-geTtKL4rlsU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP794392.RAZSByKIZuOKi7aU3_l_AjMVxKYh92gEn-geTtKL4rlsU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP794392.RAZSByKIZuOKi7aU3_l_AjMVxKYh92gEn-geTtKL4rlsU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP794392.RAZSByKIZuOKi7aU3_l_AjMVxKYh92gEn-geTtKL4rlsU130_provenance.
- NP794392.RAZSByKIZuOKi7aU3_l_AjMVxKYh92gEn-geTtKL4rlsU130_assertion description "[Autosomal recessive mutations in the ALS2 gene have been linked to juvenile-onset amyotrophic lateral sclerosis (ALS2), primary lateral sclerosis and juvenile-onset ascending hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP794392.RAZSByKIZuOKi7aU3_l_AjMVxKYh92gEn-geTtKL4rlsU130_provenance.
- NP794392.RAZSByKIZuOKi7aU3_l_AjMVxKYh92gEn-geTtKL4rlsU130_assertion evidence source_evidence_literature NP794392.RAZSByKIZuOKi7aU3_l_AjMVxKYh92gEn-geTtKL4rlsU130_provenance.
- NP794392.RAZSByKIZuOKi7aU3_l_AjMVxKYh92gEn-geTtKL4rlsU130_assertion SIO_000772 18714162 NP794392.RAZSByKIZuOKi7aU3_l_AjMVxKYh92gEn-geTtKL4rlsU130_provenance.
- NP794392.RAZSByKIZuOKi7aU3_l_AjMVxKYh92gEn-geTtKL4rlsU130_assertion wasDerivedFrom befree-20140225 NP794392.RAZSByKIZuOKi7aU3_l_AjMVxKYh92gEn-geTtKL4rlsU130_provenance.
- NP794392.RAZSByKIZuOKi7aU3_l_AjMVxKYh92gEn-geTtKL4rlsU130_assertion wasGeneratedBy ECO_0000203 NP794392.RAZSByKIZuOKi7aU3_l_AjMVxKYh92gEn-geTtKL4rlsU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP794392.RAZSByKIZuOKi7aU3_l_AjMVxKYh92gEn-geTtKL4rlsU130_provenance.