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- source_evidence_literature type ECO_0000212 NP831967.RAZDQC4d5p-9avjCbdnBkR2V8lEfd3Qyetxh-lTo3Etwo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP831967.RAZDQC4d5p-9avjCbdnBkR2V8lEfd3Qyetxh-lTo3Etwo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP831967.RAZDQC4d5p-9avjCbdnBkR2V8lEfd3Qyetxh-lTo3Etwo130_provenance.
- NP831967.RAZDQC4d5p-9avjCbdnBkR2V8lEfd3Qyetxh-lTo3Etwo130_assertion description "[We identified pathogenic mutations of human FIG4 (KIAA0274) on chromosome 6q21 in four unrelated patients with hereditary motor and sensory neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831967.RAZDQC4d5p-9avjCbdnBkR2V8lEfd3Qyetxh-lTo3Etwo130_provenance.
- NP831967.RAZDQC4d5p-9avjCbdnBkR2V8lEfd3Qyetxh-lTo3Etwo130_assertion evidence source_evidence_literature NP831967.RAZDQC4d5p-9avjCbdnBkR2V8lEfd3Qyetxh-lTo3Etwo130_provenance.
- NP831967.RAZDQC4d5p-9avjCbdnBkR2V8lEfd3Qyetxh-lTo3Etwo130_assertion SIO_000772 17572665 NP831967.RAZDQC4d5p-9avjCbdnBkR2V8lEfd3Qyetxh-lTo3Etwo130_provenance.
- NP831967.RAZDQC4d5p-9avjCbdnBkR2V8lEfd3Qyetxh-lTo3Etwo130_assertion wasDerivedFrom befree-20150227 NP831967.RAZDQC4d5p-9avjCbdnBkR2V8lEfd3Qyetxh-lTo3Etwo130_provenance.
- NP831967.RAZDQC4d5p-9avjCbdnBkR2V8lEfd3Qyetxh-lTo3Etwo130_assertion wasGeneratedBy ECO_0000203 NP831967.RAZDQC4d5p-9avjCbdnBkR2V8lEfd3Qyetxh-lTo3Etwo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP831967.RAZDQC4d5p-9avjCbdnBkR2V8lEfd3Qyetxh-lTo3Etwo130_provenance.