Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP493297.RAJCHvKM27c63fpkmp0dJVqhvBO7QGgEhFnSz--cuePcs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP493297.RAJCHvKM27c63fpkmp0dJVqhvBO7QGgEhFnSz--cuePcs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP493297.RAJCHvKM27c63fpkmp0dJVqhvBO7QGgEhFnSz--cuePcs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP493297.RAJCHvKM27c63fpkmp0dJVqhvBO7QGgEhFnSz--cuePcs130_provenance.
- NP493297.RAJCHvKM27c63fpkmp0dJVqhvBO7QGgEhFnSz--cuePcs130_assertion description "[To understand the molecular basis of the genetic defect, the gene encoding cystatin C was isolated from genomic DNA libraries made from normal tissue and the brain of an Icelandic patient with hereditary cerebral hemorrhage with amyloidosis (HCHWA-I).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493297.RAJCHvKM27c63fpkmp0dJVqhvBO7QGgEhFnSz--cuePcs130_provenance.
- NP493297.RAJCHvKM27c63fpkmp0dJVqhvBO7QGgEhFnSz--cuePcs130_assertion evidence source_evidence_literature NP493297.RAJCHvKM27c63fpkmp0dJVqhvBO7QGgEhFnSz--cuePcs130_provenance.
- NP493297.RAJCHvKM27c63fpkmp0dJVqhvBO7QGgEhFnSz--cuePcs130_assertion SIO_000772 2541223 NP493297.RAJCHvKM27c63fpkmp0dJVqhvBO7QGgEhFnSz--cuePcs130_provenance.
- NP493297.RAJCHvKM27c63fpkmp0dJVqhvBO7QGgEhFnSz--cuePcs130_assertion wasDerivedFrom befree-20140225 NP493297.RAJCHvKM27c63fpkmp0dJVqhvBO7QGgEhFnSz--cuePcs130_provenance.
- NP493297.RAJCHvKM27c63fpkmp0dJVqhvBO7QGgEhFnSz--cuePcs130_assertion wasGeneratedBy ECO_0000203 NP493297.RAJCHvKM27c63fpkmp0dJVqhvBO7QGgEhFnSz--cuePcs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP493297.RAJCHvKM27c63fpkmp0dJVqhvBO7QGgEhFnSz--cuePcs130_provenance.