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- source_evidence_literature type ECO_0000212 NP1327021.RAjVhbBq1QkIpFxhZTyP-j8jjFC1ZdoF4mqCueohcn5gw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1327021.RAjVhbBq1QkIpFxhZTyP-j8jjFC1ZdoF4mqCueohcn5gw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1327021.RAjVhbBq1QkIpFxhZTyP-j8jjFC1ZdoF4mqCueohcn5gw130_provenance.
- NP1327021.RAjVhbBq1QkIpFxhZTyP-j8jjFC1ZdoF4mqCueohcn5gw130_assertion description "[Furthermore, the linkage of mutations within the PRNP gene with phenotypic appearance of Creutzfeldt-Jakob disease and Gerstmann-Str�ussler-Scheinker syndrome points to importance of the PrP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327021.RAjVhbBq1QkIpFxhZTyP-j8jjFC1ZdoF4mqCueohcn5gw130_provenance.
- NP1327021.RAjVhbBq1QkIpFxhZTyP-j8jjFC1ZdoF4mqCueohcn5gw130_assertion evidence source_evidence_literature NP1327021.RAjVhbBq1QkIpFxhZTyP-j8jjFC1ZdoF4mqCueohcn5gw130_provenance.
- NP1327021.RAjVhbBq1QkIpFxhZTyP-j8jjFC1ZdoF4mqCueohcn5gw130_assertion SIO_000772 7922109 NP1327021.RAjVhbBq1QkIpFxhZTyP-j8jjFC1ZdoF4mqCueohcn5gw130_provenance.
- NP1327021.RAjVhbBq1QkIpFxhZTyP-j8jjFC1ZdoF4mqCueohcn5gw130_assertion wasDerivedFrom befree-2016 NP1327021.RAjVhbBq1QkIpFxhZTyP-j8jjFC1ZdoF4mqCueohcn5gw130_provenance.
- NP1327021.RAjVhbBq1QkIpFxhZTyP-j8jjFC1ZdoF4mqCueohcn5gw130_assertion wasGeneratedBy ECO_0000203 NP1327021.RAjVhbBq1QkIpFxhZTyP-j8jjFC1ZdoF4mqCueohcn5gw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1327021.RAjVhbBq1QkIpFxhZTyP-j8jjFC1ZdoF4mqCueohcn5gw130_provenance.