Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP331336.RAt20Yp0OcK_HdMWXuK6tcgSDaHhX42kQ3FJx9poK_9kc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP331336.RAt20Yp0OcK_HdMWXuK6tcgSDaHhX42kQ3FJx9poK_9kc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP331336.RAt20Yp0OcK_HdMWXuK6tcgSDaHhX42kQ3FJx9poK_9kc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP331336.RAt20Yp0OcK_HdMWXuK6tcgSDaHhX42kQ3FJx9poK_9kc130_provenance.
- befree-2016 importedOn "2016-02-19" NP331336.RAt20Yp0OcK_HdMWXuK6tcgSDaHhX42kQ3FJx9poK_9kc130_provenance.
- NP331336.RAt20Yp0OcK_HdMWXuK6tcgSDaHhX42kQ3FJx9poK_9kc130_assertion wasGeneratedBy ECO_0000203 NP331336.RAt20Yp0OcK_HdMWXuK6tcgSDaHhX42kQ3FJx9poK_9kc130_provenance.
- NP331336.RAt20Yp0OcK_HdMWXuK6tcgSDaHhX42kQ3FJx9poK_9kc130_assertion wasDerivedFrom befree-2016 NP331336.RAt20Yp0OcK_HdMWXuK6tcgSDaHhX42kQ3FJx9poK_9kc130_provenance.
- NP331336.RAt20Yp0OcK_HdMWXuK6tcgSDaHhX42kQ3FJx9poK_9kc130_assertion SIO_000772 11576738 NP331336.RAt20Yp0OcK_HdMWXuK6tcgSDaHhX42kQ3FJx9poK_9kc130_provenance.
- NP331336.RAt20Yp0OcK_HdMWXuK6tcgSDaHhX42kQ3FJx9poK_9kc130_assertion evidence source_evidence_literature NP331336.RAt20Yp0OcK_HdMWXuK6tcgSDaHhX42kQ3FJx9poK_9kc130_provenance.
- NP331336.RAt20Yp0OcK_HdMWXuK6tcgSDaHhX42kQ3FJx9poK_9kc130_assertion description "[PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP331336.RAt20Yp0OcK_HdMWXuK6tcgSDaHhX42kQ3FJx9poK_9kc130_provenance.