Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1380074.RAGnfgzarUJwp29bL5b5nsOmP1Zxw4U6Op7Ace3L6xVvo130_assertion> ?p ?o ?g. }
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- NP1380074.RAGnfgzarUJwp29bL5b5nsOmP1Zxw4U6Op7Ace3L6xVvo130_assertion type Assertion NP1380074.RAGnfgzarUJwp29bL5b5nsOmP1Zxw4U6Op7Ace3L6xVvo130_head.
- NP1380074.RAGnfgzarUJwp29bL5b5nsOmP1Zxw4U6Op7Ace3L6xVvo130_assertion description "[We investigated the allelic origin of PrP(res) in brains of subjects heterozygous for the D178N mutation linked to fatal familial insomnia (FFI) and a subtype of Creutzfeldt-Jakob disease (CJD178), as well as for insertional mutations associated with another CJD subtype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1380074.RAGnfgzarUJwp29bL5b5nsOmP1Zxw4U6Op7Ace3L6xVvo130_provenance.
- NP1380074.RAGnfgzarUJwp29bL5b5nsOmP1Zxw4U6Op7Ace3L6xVvo130_assertion evidence source_evidence_literature NP1380074.RAGnfgzarUJwp29bL5b5nsOmP1Zxw4U6Op7Ace3L6xVvo130_provenance.
- NP1380074.RAGnfgzarUJwp29bL5b5nsOmP1Zxw4U6Op7Ace3L6xVvo130_assertion SIO_000772 9288728 NP1380074.RAGnfgzarUJwp29bL5b5nsOmP1Zxw4U6Op7Ace3L6xVvo130_provenance.
- NP1380074.RAGnfgzarUJwp29bL5b5nsOmP1Zxw4U6Op7Ace3L6xVvo130_assertion wasDerivedFrom befree-2016 NP1380074.RAGnfgzarUJwp29bL5b5nsOmP1Zxw4U6Op7Ace3L6xVvo130_provenance.
- NP1380074.RAGnfgzarUJwp29bL5b5nsOmP1Zxw4U6Op7Ace3L6xVvo130_assertion wasGeneratedBy ECO_0000203 NP1380074.RAGnfgzarUJwp29bL5b5nsOmP1Zxw4U6Op7Ace3L6xVvo130_provenance.