Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP30622.RAShQSxmy50-C9z8IZ5v590Trp_UWSFDcAy7Vs9XbMa0s130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP30622.RAShQSxmy50-C9z8IZ5v590Trp_UWSFDcAy7Vs9XbMa0s130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP30622.RAShQSxmy50-C9z8IZ5v590Trp_UWSFDcAy7Vs9XbMa0s130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP30622.RAShQSxmy50-C9z8IZ5v590Trp_UWSFDcAy7Vs9XbMa0s130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP30622.RAShQSxmy50-C9z8IZ5v590Trp_UWSFDcAy7Vs9XbMa0s130_provenance.
- NP30622.RAShQSxmy50-C9z8IZ5v590Trp_UWSFDcAy7Vs9XbMa0s130_assertion wasGeneratedBy ECO_0000218 NP30622.RAShQSxmy50-C9z8IZ5v590Trp_UWSFDcAy7Vs9XbMa0s130_provenance.
- NP30622.RAShQSxmy50-C9z8IZ5v590Trp_UWSFDcAy7Vs9XbMa0s130_assertion wasDerivedFrom ctd_human-20150221 NP30622.RAShQSxmy50-C9z8IZ5v590Trp_UWSFDcAy7Vs9XbMa0s130_provenance.
- NP30622.RAShQSxmy50-C9z8IZ5v590Trp_UWSFDcAy7Vs9XbMa0s130_assertion SIO_000772 11951178 NP30622.RAShQSxmy50-C9z8IZ5v590Trp_UWSFDcAy7Vs9XbMa0s130_provenance.
- NP30622.RAShQSxmy50-C9z8IZ5v590Trp_UWSFDcAy7Vs9XbMa0s130_assertion evidence source_evidence_curated NP30622.RAShQSxmy50-C9z8IZ5v590Trp_UWSFDcAy7Vs9XbMa0s130_provenance.
- NP30622.RAShQSxmy50-C9z8IZ5v590Trp_UWSFDcAy7Vs9XbMa0s130_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." NP30622.RAShQSxmy50-C9z8IZ5v590Trp_UWSFDcAy7Vs9XbMa0s130_provenance.