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- source_evidence_literature type ECO_0000212 NP1327019.RAtkSZdCwTWiSzaO3dUREj0X9ntpnEB6CsMAuG_VyyPlk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1327019.RAtkSZdCwTWiSzaO3dUREj0X9ntpnEB6CsMAuG_VyyPlk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1327019.RAtkSZdCwTWiSzaO3dUREj0X9ntpnEB6CsMAuG_VyyPlk130_provenance.
- NP1327019.RAtkSZdCwTWiSzaO3dUREj0X9ntpnEB6CsMAuG_VyyPlk130_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." NP1327019.RAtkSZdCwTWiSzaO3dUREj0X9ntpnEB6CsMAuG_VyyPlk130_provenance.
- NP1327019.RAtkSZdCwTWiSzaO3dUREj0X9ntpnEB6CsMAuG_VyyPlk130_assertion evidence source_evidence_literature NP1327019.RAtkSZdCwTWiSzaO3dUREj0X9ntpnEB6CsMAuG_VyyPlk130_provenance.
- NP1327019.RAtkSZdCwTWiSzaO3dUREj0X9ntpnEB6CsMAuG_VyyPlk130_assertion SIO_000772 7922109 NP1327019.RAtkSZdCwTWiSzaO3dUREj0X9ntpnEB6CsMAuG_VyyPlk130_provenance.
- NP1327019.RAtkSZdCwTWiSzaO3dUREj0X9ntpnEB6CsMAuG_VyyPlk130_assertion wasDerivedFrom befree-2016 NP1327019.RAtkSZdCwTWiSzaO3dUREj0X9ntpnEB6CsMAuG_VyyPlk130_provenance.
- NP1327019.RAtkSZdCwTWiSzaO3dUREj0X9ntpnEB6CsMAuG_VyyPlk130_assertion wasGeneratedBy ECO_0000203 NP1327019.RAtkSZdCwTWiSzaO3dUREj0X9ntpnEB6CsMAuG_VyyPlk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1327019.RAtkSZdCwTWiSzaO3dUREj0X9ntpnEB6CsMAuG_VyyPlk130_provenance.