Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP828924.RA_Wa6Iye9S0B7Hp6BkxqY_aSnFMSbdRvdI9HROPmd3XY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP828924.RA_Wa6Iye9S0B7Hp6BkxqY_aSnFMSbdRvdI9HROPmd3XY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP828924.RA_Wa6Iye9S0B7Hp6BkxqY_aSnFMSbdRvdI9HROPmd3XY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP828924.RA_Wa6Iye9S0B7Hp6BkxqY_aSnFMSbdRvdI9HROPmd3XY130_provenance.
- NP828924.RA_Wa6Iye9S0B7Hp6BkxqY_aSnFMSbdRvdI9HROPmd3XY130_assertion description "[Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are responsible for a severe neurological disorder known as Unverricht-Lundborg disease (EPM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP828924.RA_Wa6Iye9S0B7Hp6BkxqY_aSnFMSbdRvdI9HROPmd3XY130_provenance.
- NP828924.RA_Wa6Iye9S0B7Hp6BkxqY_aSnFMSbdRvdI9HROPmd3XY130_assertion evidence source_evidence_literature NP828924.RA_Wa6Iye9S0B7Hp6BkxqY_aSnFMSbdRvdI9HROPmd3XY130_provenance.
- NP828924.RA_Wa6Iye9S0B7Hp6BkxqY_aSnFMSbdRvdI9HROPmd3XY130_assertion SIO_000772 9806543 NP828924.RA_Wa6Iye9S0B7Hp6BkxqY_aSnFMSbdRvdI9HROPmd3XY130_provenance.
- NP828924.RA_Wa6Iye9S0B7Hp6BkxqY_aSnFMSbdRvdI9HROPmd3XY130_assertion wasDerivedFrom befree-20140225 NP828924.RA_Wa6Iye9S0B7Hp6BkxqY_aSnFMSbdRvdI9HROPmd3XY130_provenance.
- NP828924.RA_Wa6Iye9S0B7Hp6BkxqY_aSnFMSbdRvdI9HROPmd3XY130_assertion wasGeneratedBy ECO_0000203 NP828924.RA_Wa6Iye9S0B7Hp6BkxqY_aSnFMSbdRvdI9HROPmd3XY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP828924.RA_Wa6Iye9S0B7Hp6BkxqY_aSnFMSbdRvdI9HROPmd3XY130_provenance.