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- source_evidence_literature type ECO_0000212 NP915729.RAxCnxmEpwebq6iK6AJOPur22DCmkm8WfngSstmRnq8nw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP915729.RAxCnxmEpwebq6iK6AJOPur22DCmkm8WfngSstmRnq8nw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP915729.RAxCnxmEpwebq6iK6AJOPur22DCmkm8WfngSstmRnq8nw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP915729.RAxCnxmEpwebq6iK6AJOPur22DCmkm8WfngSstmRnq8nw130_provenance.
- NP915729.RAxCnxmEpwebq6iK6AJOPur22DCmkm8WfngSstmRnq8nw130_assertion wasGeneratedBy ECO_0000203 NP915729.RAxCnxmEpwebq6iK6AJOPur22DCmkm8WfngSstmRnq8nw130_provenance.
- NP915729.RAxCnxmEpwebq6iK6AJOPur22DCmkm8WfngSstmRnq8nw130_assertion wasDerivedFrom befree-20150227 NP915729.RAxCnxmEpwebq6iK6AJOPur22DCmkm8WfngSstmRnq8nw130_provenance.
- NP915729.RAxCnxmEpwebq6iK6AJOPur22DCmkm8WfngSstmRnq8nw130_assertion SIO_000772 23297359 NP915729.RAxCnxmEpwebq6iK6AJOPur22DCmkm8WfngSstmRnq8nw130_provenance.
- NP915729.RAxCnxmEpwebq6iK6AJOPur22DCmkm8WfngSstmRnq8nw130_assertion evidence source_evidence_literature NP915729.RAxCnxmEpwebq6iK6AJOPur22DCmkm8WfngSstmRnq8nw130_provenance.
- NP915729.RAxCnxmEpwebq6iK6AJOPur22DCmkm8WfngSstmRnq8nw130_assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915729.RAxCnxmEpwebq6iK6AJOPur22DCmkm8WfngSstmRnq8nw130_provenance.