Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP207926.RAcxd4NPK6iQQrT8Bu2-KrPmCclgrX1RLthnA_0bFHwM8130_assertion> ?p ?o ?g. }
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- NP207926.RAcxd4NPK6iQQrT8Bu2-KrPmCclgrX1RLthnA_0bFHwM8130_assertion type Assertion NP207926.RAcxd4NPK6iQQrT8Bu2-KrPmCclgrX1RLthnA_0bFHwM8130_head.
- NP207926.RAcxd4NPK6iQQrT8Bu2-KrPmCclgrX1RLthnA_0bFHwM8130_assertion wasGeneratedBy ECO_0000203 NP207926.RAcxd4NPK6iQQrT8Bu2-KrPmCclgrX1RLthnA_0bFHwM8130_provenance.
- NP207926.RAcxd4NPK6iQQrT8Bu2-KrPmCclgrX1RLthnA_0bFHwM8130_assertion wasDerivedFrom lhgdn-20090331 NP207926.RAcxd4NPK6iQQrT8Bu2-KrPmCclgrX1RLthnA_0bFHwM8130_provenance.
- NP207926.RAcxd4NPK6iQQrT8Bu2-KrPmCclgrX1RLthnA_0bFHwM8130_assertion SIO_000772 15557533 NP207926.RAcxd4NPK6iQQrT8Bu2-KrPmCclgrX1RLthnA_0bFHwM8130_provenance.
- NP207926.RAcxd4NPK6iQQrT8Bu2-KrPmCclgrX1RLthnA_0bFHwM8130_assertion evidence source_evidence_literature NP207926.RAcxd4NPK6iQQrT8Bu2-KrPmCclgrX1RLthnA_0bFHwM8130_provenance.
- NP207926.RAcxd4NPK6iQQrT8Bu2-KrPmCclgrX1RLthnA_0bFHwM8130_assertion description "[A 72 bp insertion between codons 51 & 91 consisting of a three-time octapeptide repeat (R3g, R2, R2), a codon 219 Lys/Lys polymorphism, and a codon 129 Met/Met polymorphism were found in a sporadic case of Creutzfeldt-Jakob disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207926.RAcxd4NPK6iQQrT8Bu2-KrPmCclgrX1RLthnA_0bFHwM8130_provenance.