Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP401404.RAGRvLjrWJbmdnVuXXIAxhLnDN0x1_EoKAqiQvwNGMobc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP401404.RAGRvLjrWJbmdnVuXXIAxhLnDN0x1_EoKAqiQvwNGMobc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP401404.RAGRvLjrWJbmdnVuXXIAxhLnDN0x1_EoKAqiQvwNGMobc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP401404.RAGRvLjrWJbmdnVuXXIAxhLnDN0x1_EoKAqiQvwNGMobc130_provenance.
- NP401404.RAGRvLjrWJbmdnVuXXIAxhLnDN0x1_EoKAqiQvwNGMobc130_assertion description "[Mutations in the gene encoding cystatin B (CSTB), a cysteine protease inhibitor, are responsible for the primary defect in Unverricht-Lundborg disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401404.RAGRvLjrWJbmdnVuXXIAxhLnDN0x1_EoKAqiQvwNGMobc130_provenance.
- NP401404.RAGRvLjrWJbmdnVuXXIAxhLnDN0x1_EoKAqiQvwNGMobc130_assertion evidence source_evidence_literature NP401404.RAGRvLjrWJbmdnVuXXIAxhLnDN0x1_EoKAqiQvwNGMobc130_provenance.
- NP401404.RAGRvLjrWJbmdnVuXXIAxhLnDN0x1_EoKAqiQvwNGMobc130_assertion SIO_000772 12853462 NP401404.RAGRvLjrWJbmdnVuXXIAxhLnDN0x1_EoKAqiQvwNGMobc130_provenance.
- NP401404.RAGRvLjrWJbmdnVuXXIAxhLnDN0x1_EoKAqiQvwNGMobc130_assertion wasDerivedFrom befree-2016 NP401404.RAGRvLjrWJbmdnVuXXIAxhLnDN0x1_EoKAqiQvwNGMobc130_provenance.
- NP401404.RAGRvLjrWJbmdnVuXXIAxhLnDN0x1_EoKAqiQvwNGMobc130_assertion wasGeneratedBy ECO_0000203 NP401404.RAGRvLjrWJbmdnVuXXIAxhLnDN0x1_EoKAqiQvwNGMobc130_provenance.
- befree-2016 importedOn "2016-02-19" NP401404.RAGRvLjrWJbmdnVuXXIAxhLnDN0x1_EoKAqiQvwNGMobc130_provenance.