Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP882886.RACGkSHFTDtR66ZfSSlvuq5emI-laMBtpUxEOW19YAuGE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP882886.RACGkSHFTDtR66ZfSSlvuq5emI-laMBtpUxEOW19YAuGE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP882886.RACGkSHFTDtR66ZfSSlvuq5emI-laMBtpUxEOW19YAuGE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP882886.RACGkSHFTDtR66ZfSSlvuq5emI-laMBtpUxEOW19YAuGE130_provenance.
- NP882886.RACGkSHFTDtR66ZfSSlvuq5emI-laMBtpUxEOW19YAuGE130_assertion description "[The protein sacsin, which is mutated in the early-onset neurodegenerative disease autosomal recessive spastic ataxia of Charlevoix-Saguenay, is a node in this interactome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP882886.RACGkSHFTDtR66ZfSSlvuq5emI-laMBtpUxEOW19YAuGE130_provenance.
- NP882886.RACGkSHFTDtR66ZfSSlvuq5emI-laMBtpUxEOW19YAuGE130_assertion evidence source_evidence_literature NP882886.RACGkSHFTDtR66ZfSSlvuq5emI-laMBtpUxEOW19YAuGE130_provenance.
- NP882886.RACGkSHFTDtR66ZfSSlvuq5emI-laMBtpUxEOW19YAuGE130_assertion SIO_000772 19208651 NP882886.RACGkSHFTDtR66ZfSSlvuq5emI-laMBtpUxEOW19YAuGE130_provenance.
- NP882886.RACGkSHFTDtR66ZfSSlvuq5emI-laMBtpUxEOW19YAuGE130_assertion wasDerivedFrom befree-20150227 NP882886.RACGkSHFTDtR66ZfSSlvuq5emI-laMBtpUxEOW19YAuGE130_provenance.
- NP882886.RACGkSHFTDtR66ZfSSlvuq5emI-laMBtpUxEOW19YAuGE130_assertion wasGeneratedBy ECO_0000203 NP882886.RACGkSHFTDtR66ZfSSlvuq5emI-laMBtpUxEOW19YAuGE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP882886.RACGkSHFTDtR66ZfSSlvuq5emI-laMBtpUxEOW19YAuGE130_provenance.