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- NP762296.RAAn0WhJz97Ue56pjfNIjlFT3CSpPPLW4QBpTR2xfA0bE130_assertion type Assertion NP762296.RAAn0WhJz97Ue56pjfNIjlFT3CSpPPLW4QBpTR2xfA0bE130_head.
- NP762296.RAAn0WhJz97Ue56pjfNIjlFT3CSpPPLW4QBpTR2xfA0bE130_assertion description "[DYT16 dystonia is a novel recessive form of EO-PD, recently described in few patients, caused by mutations in the PRKRA gene located at chromosome 2q31.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762296.RAAn0WhJz97Ue56pjfNIjlFT3CSpPPLW4QBpTR2xfA0bE130_provenance.
- NP762296.RAAn0WhJz97Ue56pjfNIjlFT3CSpPPLW4QBpTR2xfA0bE130_assertion evidence source_evidence_literature NP762296.RAAn0WhJz97Ue56pjfNIjlFT3CSpPPLW4QBpTR2xfA0bE130_provenance.
- NP762296.RAAn0WhJz97Ue56pjfNIjlFT3CSpPPLW4QBpTR2xfA0bE130_assertion SIO_000772 19157930 NP762296.RAAn0WhJz97Ue56pjfNIjlFT3CSpPPLW4QBpTR2xfA0bE130_provenance.
- NP762296.RAAn0WhJz97Ue56pjfNIjlFT3CSpPPLW4QBpTR2xfA0bE130_assertion wasDerivedFrom befree-20140225 NP762296.RAAn0WhJz97Ue56pjfNIjlFT3CSpPPLW4QBpTR2xfA0bE130_provenance.
- NP762296.RAAn0WhJz97Ue56pjfNIjlFT3CSpPPLW4QBpTR2xfA0bE130_assertion wasGeneratedBy ECO_0000203 NP762296.RAAn0WhJz97Ue56pjfNIjlFT3CSpPPLW4QBpTR2xfA0bE130_provenance.