Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP439956.RAxk7n6JfvAsEs5alC4uh8xQKmtZdp_VhUqIeP0HD-SBs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP439956.RAxk7n6JfvAsEs5alC4uh8xQKmtZdp_VhUqIeP0HD-SBs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP439956.RAxk7n6JfvAsEs5alC4uh8xQKmtZdp_VhUqIeP0HD-SBs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP439956.RAxk7n6JfvAsEs5alC4uh8xQKmtZdp_VhUqIeP0HD-SBs130_provenance.
- NP439956.RAxk7n6JfvAsEs5alC4uh8xQKmtZdp_VhUqIeP0HD-SBs130_assertion description "[We sequenced UBQLN2 in 130 French patients with familial ALS (FALS) and absence of male-to-male transmission and the PXX domain in 240 more patients with sporadic ALS (SALS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP439956.RAxk7n6JfvAsEs5alC4uh8xQKmtZdp_VhUqIeP0HD-SBs130_provenance.
- NP439956.RAxk7n6JfvAsEs5alC4uh8xQKmtZdp_VhUqIeP0HD-SBs130_assertion evidence source_evidence_literature NP439956.RAxk7n6JfvAsEs5alC4uh8xQKmtZdp_VhUqIeP0HD-SBs130_provenance.
- NP439956.RAxk7n6JfvAsEs5alC4uh8xQKmtZdp_VhUqIeP0HD-SBs130_assertion SIO_000772 22169395 NP439956.RAxk7n6JfvAsEs5alC4uh8xQKmtZdp_VhUqIeP0HD-SBs130_provenance.
- NP439956.RAxk7n6JfvAsEs5alC4uh8xQKmtZdp_VhUqIeP0HD-SBs130_assertion wasDerivedFrom befree-20140225 NP439956.RAxk7n6JfvAsEs5alC4uh8xQKmtZdp_VhUqIeP0HD-SBs130_provenance.
- NP439956.RAxk7n6JfvAsEs5alC4uh8xQKmtZdp_VhUqIeP0HD-SBs130_assertion wasGeneratedBy ECO_0000203 NP439956.RAxk7n6JfvAsEs5alC4uh8xQKmtZdp_VhUqIeP0HD-SBs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP439956.RAxk7n6JfvAsEs5alC4uh8xQKmtZdp_VhUqIeP0HD-SBs130_provenance.