Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP261687.RAEpf23QIPlUbLZssPKtRjhuZ41hT_cgIvVx2sPu4SFK0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP261687.RAEpf23QIPlUbLZssPKtRjhuZ41hT_cgIvVx2sPu4SFK0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP261687.RAEpf23QIPlUbLZssPKtRjhuZ41hT_cgIvVx2sPu4SFK0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP261687.RAEpf23QIPlUbLZssPKtRjhuZ41hT_cgIvVx2sPu4SFK0130_provenance.
- NP261687.RAEpf23QIPlUbLZssPKtRjhuZ41hT_cgIvVx2sPu4SFK0130_assertion description "[The distribution of an Arg-His polymorphism in the LMP 2 gene and a G/T polymorphism in the LMP 7 gene, both of which lead to the presence of an HhaI restriction site, were investigated in a population based case control and family based study in patients with Graves' disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261687.RAEpf23QIPlUbLZssPKtRjhuZ41hT_cgIvVx2sPu4SFK0130_provenance.
- NP261687.RAEpf23QIPlUbLZssPKtRjhuZ41hT_cgIvVx2sPu4SFK0130_assertion evidence source_evidence_literature NP261687.RAEpf23QIPlUbLZssPKtRjhuZ41hT_cgIvVx2sPu4SFK0130_provenance.
- NP261687.RAEpf23QIPlUbLZssPKtRjhuZ41hT_cgIvVx2sPu4SFK0130_assertion SIO_000772 10468973 NP261687.RAEpf23QIPlUbLZssPKtRjhuZ41hT_cgIvVx2sPu4SFK0130_provenance.
- NP261687.RAEpf23QIPlUbLZssPKtRjhuZ41hT_cgIvVx2sPu4SFK0130_assertion wasDerivedFrom befree-2016 NP261687.RAEpf23QIPlUbLZssPKtRjhuZ41hT_cgIvVx2sPu4SFK0130_provenance.
- NP261687.RAEpf23QIPlUbLZssPKtRjhuZ41hT_cgIvVx2sPu4SFK0130_assertion wasGeneratedBy ECO_0000203 NP261687.RAEpf23QIPlUbLZssPKtRjhuZ41hT_cgIvVx2sPu4SFK0130_provenance.
- befree-2016 importedOn "2016-02-19" NP261687.RAEpf23QIPlUbLZssPKtRjhuZ41hT_cgIvVx2sPu4SFK0130_provenance.