Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP412608.RAb2EG7BP44nvZ-LyefCKa-QeNIy_KAi8TLdQLGOjuUoY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP412608.RAb2EG7BP44nvZ-LyefCKa-QeNIy_KAi8TLdQLGOjuUoY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP412608.RAb2EG7BP44nvZ-LyefCKa-QeNIy_KAi8TLdQLGOjuUoY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP412608.RAb2EG7BP44nvZ-LyefCKa-QeNIy_KAi8TLdQLGOjuUoY130_provenance.
- NP412608.RAb2EG7BP44nvZ-LyefCKa-QeNIy_KAi8TLdQLGOjuUoY130_assertion description "[Progressive myoclonus epilepsy 1 (EPM1) or Unverricht-Lundborg disease is a human autosomal recessive neurodegenerative disorder caused by mutations in cystatin B (CSTB).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412608.RAb2EG7BP44nvZ-LyefCKa-QeNIy_KAi8TLdQLGOjuUoY130_provenance.
- NP412608.RAb2EG7BP44nvZ-LyefCKa-QeNIy_KAi8TLdQLGOjuUoY130_assertion evidence source_evidence_literature NP412608.RAb2EG7BP44nvZ-LyefCKa-QeNIy_KAi8TLdQLGOjuUoY130_provenance.
- NP412608.RAb2EG7BP44nvZ-LyefCKa-QeNIy_KAi8TLdQLGOjuUoY130_assertion SIO_000772 14526183 NP412608.RAb2EG7BP44nvZ-LyefCKa-QeNIy_KAi8TLdQLGOjuUoY130_provenance.
- NP412608.RAb2EG7BP44nvZ-LyefCKa-QeNIy_KAi8TLdQLGOjuUoY130_assertion wasDerivedFrom befree-20140225 NP412608.RAb2EG7BP44nvZ-LyefCKa-QeNIy_KAi8TLdQLGOjuUoY130_provenance.
- NP412608.RAb2EG7BP44nvZ-LyefCKa-QeNIy_KAi8TLdQLGOjuUoY130_assertion wasGeneratedBy ECO_0000203 NP412608.RAb2EG7BP44nvZ-LyefCKa-QeNIy_KAi8TLdQLGOjuUoY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP412608.RAb2EG7BP44nvZ-LyefCKa-QeNIy_KAi8TLdQLGOjuUoY130_provenance.