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- source_evidence_literature type ECO_0000212 NP672524.RAhweN_Mccox3Hp05Ea7OovqKey_m9QjE5k8GqLVzDgLU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP672524.RAhweN_Mccox3Hp05Ea7OovqKey_m9QjE5k8GqLVzDgLU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP672524.RAhweN_Mccox3Hp05Ea7OovqKey_m9QjE5k8GqLVzDgLU130_provenance.
- NP672524.RAhweN_Mccox3Hp05Ea7OovqKey_m9QjE5k8GqLVzDgLU130_assertion description "[Mutations in the SH3TC2 gene are a frequent cause of demyelinating hereditary neuropathy among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672524.RAhweN_Mccox3Hp05Ea7OovqKey_m9QjE5k8GqLVzDgLU130_provenance.
- NP672524.RAhweN_Mccox3Hp05Ea7OovqKey_m9QjE5k8GqLVzDgLU130_assertion evidence source_evidence_literature NP672524.RAhweN_Mccox3Hp05Ea7OovqKey_m9QjE5k8GqLVzDgLU130_provenance.
- NP672524.RAhweN_Mccox3Hp05Ea7OovqKey_m9QjE5k8GqLVzDgLU130_assertion SIO_000772 21291453 NP672524.RAhweN_Mccox3Hp05Ea7OovqKey_m9QjE5k8GqLVzDgLU130_provenance.
- NP672524.RAhweN_Mccox3Hp05Ea7OovqKey_m9QjE5k8GqLVzDgLU130_assertion wasDerivedFrom befree-20140225 NP672524.RAhweN_Mccox3Hp05Ea7OovqKey_m9QjE5k8GqLVzDgLU130_provenance.
- NP672524.RAhweN_Mccox3Hp05Ea7OovqKey_m9QjE5k8GqLVzDgLU130_assertion wasGeneratedBy ECO_0000203 NP672524.RAhweN_Mccox3Hp05Ea7OovqKey_m9QjE5k8GqLVzDgLU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP672524.RAhweN_Mccox3Hp05Ea7OovqKey_m9QjE5k8GqLVzDgLU130_provenance.