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- source_evidence_literature type ECO_0000212 NP684835.RATUaBygmWuzPeVFa_QZbN57ALmnJObsyqL_s9qjA_bzY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP684835.RATUaBygmWuzPeVFa_QZbN57ALmnJObsyqL_s9qjA_bzY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP684835.RATUaBygmWuzPeVFa_QZbN57ALmnJObsyqL_s9qjA_bzY130_provenance.
- NP684835.RATUaBygmWuzPeVFa_QZbN57ALmnJObsyqL_s9qjA_bzY130_assertion description "[Myelin protein zero gene (MPZ) mutations usually cause a demyelinating variant of Charcot-Marie-Tooth disease type 1B (CMT1B), but there is a wide spectrum of phenotypic manifestation of these mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP684835.RATUaBygmWuzPeVFa_QZbN57ALmnJObsyqL_s9qjA_bzY130_provenance.
- NP684835.RATUaBygmWuzPeVFa_QZbN57ALmnJObsyqL_s9qjA_bzY130_assertion evidence source_evidence_literature NP684835.RATUaBygmWuzPeVFa_QZbN57ALmnJObsyqL_s9qjA_bzY130_provenance.
- NP684835.RATUaBygmWuzPeVFa_QZbN57ALmnJObsyqL_s9qjA_bzY130_assertion SIO_000772 18663734 NP684835.RATUaBygmWuzPeVFa_QZbN57ALmnJObsyqL_s9qjA_bzY130_provenance.
- NP684835.RATUaBygmWuzPeVFa_QZbN57ALmnJObsyqL_s9qjA_bzY130_assertion wasDerivedFrom befree-2016 NP684835.RATUaBygmWuzPeVFa_QZbN57ALmnJObsyqL_s9qjA_bzY130_provenance.
- NP684835.RATUaBygmWuzPeVFa_QZbN57ALmnJObsyqL_s9qjA_bzY130_assertion wasGeneratedBy ECO_0000203 NP684835.RATUaBygmWuzPeVFa_QZbN57ALmnJObsyqL_s9qjA_bzY130_provenance.
- befree-2016 importedOn "2016-02-19" NP684835.RATUaBygmWuzPeVFa_QZbN57ALmnJObsyqL_s9qjA_bzY130_provenance.