Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_provenance.
- NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_assertion wasGeneratedBy ECO_0000218 NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_provenance.
- NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_assertion wasDerivedFrom ctd_human-2016 NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_provenance.
- NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_assertion SIO_000772 11951178 NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_provenance.
- NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_assertion evidence source_evidence_curated NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_provenance.
- NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_assertion description "[Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_provenance.