Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP578487.RAs69KIQKElnPAI0SZcW3OXy_z-lJ3jEfh_G2s4k_ITa4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP578487.RAs69KIQKElnPAI0SZcW3OXy_z-lJ3jEfh_G2s4k_ITa4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP578487.RAs69KIQKElnPAI0SZcW3OXy_z-lJ3jEfh_G2s4k_ITa4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP578487.RAs69KIQKElnPAI0SZcW3OXy_z-lJ3jEfh_G2s4k_ITa4130_provenance.
- NP578487.RAs69KIQKElnPAI0SZcW3OXy_z-lJ3jEfh_G2s4k_ITa4130_assertion description "[Mutations in UBQLN2 encoding ubiquilin-2 have recently been identified in families with dominant X-linked juvenile and adult-onset amyotrophic lateral sclerosis (ALS) and ALS/dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP578487.RAs69KIQKElnPAI0SZcW3OXy_z-lJ3jEfh_G2s4k_ITa4130_provenance.
- NP578487.RAs69KIQKElnPAI0SZcW3OXy_z-lJ3jEfh_G2s4k_ITa4130_assertion evidence source_evidence_literature NP578487.RAs69KIQKElnPAI0SZcW3OXy_z-lJ3jEfh_G2s4k_ITa4130_provenance.
- NP578487.RAs69KIQKElnPAI0SZcW3OXy_z-lJ3jEfh_G2s4k_ITa4130_assertion SIO_000772 22169395 NP578487.RAs69KIQKElnPAI0SZcW3OXy_z-lJ3jEfh_G2s4k_ITa4130_provenance.
- NP578487.RAs69KIQKElnPAI0SZcW3OXy_z-lJ3jEfh_G2s4k_ITa4130_assertion wasDerivedFrom befree-20140225 NP578487.RAs69KIQKElnPAI0SZcW3OXy_z-lJ3jEfh_G2s4k_ITa4130_provenance.
- NP578487.RAs69KIQKElnPAI0SZcW3OXy_z-lJ3jEfh_G2s4k_ITa4130_assertion wasGeneratedBy ECO_0000203 NP578487.RAs69KIQKElnPAI0SZcW3OXy_z-lJ3jEfh_G2s4k_ITa4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP578487.RAs69KIQKElnPAI0SZcW3OXy_z-lJ3jEfh_G2s4k_ITa4130_provenance.