Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP500145.RASPN79hgWMsIjnvyaCJgRz1436-eNx8M1beEYfGntFdg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP500145.RASPN79hgWMsIjnvyaCJgRz1436-eNx8M1beEYfGntFdg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP500145.RASPN79hgWMsIjnvyaCJgRz1436-eNx8M1beEYfGntFdg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP500145.RASPN79hgWMsIjnvyaCJgRz1436-eNx8M1beEYfGntFdg130_provenance.
- NP500145.RASPN79hgWMsIjnvyaCJgRz1436-eNx8M1beEYfGntFdg130_assertion description "[Identification of three mutations in the Cu,Zn-superoxide dismutase (Cu,Zn-SOD) gene with familial amyotrophic lateral sclerosis: transduction of human Cu,Zn-SOD into PC12 cells by HIV-1 TAT protein basic domain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500145.RASPN79hgWMsIjnvyaCJgRz1436-eNx8M1beEYfGntFdg130_provenance.
- NP500145.RASPN79hgWMsIjnvyaCJgRz1436-eNx8M1beEYfGntFdg130_assertion evidence source_evidence_literature NP500145.RASPN79hgWMsIjnvyaCJgRz1436-eNx8M1beEYfGntFdg130_provenance.
- NP500145.RASPN79hgWMsIjnvyaCJgRz1436-eNx8M1beEYfGntFdg130_assertion SIO_000772 15965076 NP500145.RASPN79hgWMsIjnvyaCJgRz1436-eNx8M1beEYfGntFdg130_provenance.
- NP500145.RASPN79hgWMsIjnvyaCJgRz1436-eNx8M1beEYfGntFdg130_assertion wasDerivedFrom befree-2016 NP500145.RASPN79hgWMsIjnvyaCJgRz1436-eNx8M1beEYfGntFdg130_provenance.
- NP500145.RASPN79hgWMsIjnvyaCJgRz1436-eNx8M1beEYfGntFdg130_assertion wasGeneratedBy ECO_0000203 NP500145.RASPN79hgWMsIjnvyaCJgRz1436-eNx8M1beEYfGntFdg130_provenance.
- befree-2016 importedOn "2016-02-19" NP500145.RASPN79hgWMsIjnvyaCJgRz1436-eNx8M1beEYfGntFdg130_provenance.