Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP907482.RA6-GCmKqgQa3Dk3sdAjyjilTUFFR9NPm2uxhQCQuAwos130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP907482.RA6-GCmKqgQa3Dk3sdAjyjilTUFFR9NPm2uxhQCQuAwos130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP907482.RA6-GCmKqgQa3Dk3sdAjyjilTUFFR9NPm2uxhQCQuAwos130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP907482.RA6-GCmKqgQa3Dk3sdAjyjilTUFFR9NPm2uxhQCQuAwos130_provenance.
- NP907482.RA6-GCmKqgQa3Dk3sdAjyjilTUFFR9NPm2uxhQCQuAwos130_assertion description "[The ALS2 gene, recently found mutated in consanguineous Arabic families with either an ALS2 phenotype or a juvenile-onset primary lateral sclerosis, was analyzed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP907482.RA6-GCmKqgQa3Dk3sdAjyjilTUFFR9NPm2uxhQCQuAwos130_provenance.
- NP907482.RA6-GCmKqgQa3Dk3sdAjyjilTUFFR9NPm2uxhQCQuAwos130_assertion evidence source_evidence_literature NP907482.RA6-GCmKqgQa3Dk3sdAjyjilTUFFR9NPm2uxhQCQuAwos130_provenance.
- NP907482.RA6-GCmKqgQa3Dk3sdAjyjilTUFFR9NPm2uxhQCQuAwos130_assertion SIO_000772 12601111 NP907482.RA6-GCmKqgQa3Dk3sdAjyjilTUFFR9NPm2uxhQCQuAwos130_provenance.
- NP907482.RA6-GCmKqgQa3Dk3sdAjyjilTUFFR9NPm2uxhQCQuAwos130_assertion wasDerivedFrom befree-20140225 NP907482.RA6-GCmKqgQa3Dk3sdAjyjilTUFFR9NPm2uxhQCQuAwos130_provenance.
- NP907482.RA6-GCmKqgQa3Dk3sdAjyjilTUFFR9NPm2uxhQCQuAwos130_assertion wasGeneratedBy ECO_0000203 NP907482.RA6-GCmKqgQa3Dk3sdAjyjilTUFFR9NPm2uxhQCQuAwos130_provenance.
- befree-20140225 importedOn "2014-02-25" NP907482.RA6-GCmKqgQa3Dk3sdAjyjilTUFFR9NPm2uxhQCQuAwos130_provenance.