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- source_evidence_literature type ECO_0000212 NP914547.RACJZPikl6q9ea2M7Qk2hVs6MUen1UVpF-JLxkgi4l7PA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914547.RACJZPikl6q9ea2M7Qk2hVs6MUen1UVpF-JLxkgi4l7PA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914547.RACJZPikl6q9ea2M7Qk2hVs6MUen1UVpF-JLxkgi4l7PA130_provenance.
- NP914547.RACJZPikl6q9ea2M7Qk2hVs6MUen1UVpF-JLxkgi4l7PA130_assertion description "[Many novel ATP1A2 mutations were identified in patients with familial and sporadic hemiplegic migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914547.RACJZPikl6q9ea2M7Qk2hVs6MUen1UVpF-JLxkgi4l7PA130_provenance.
- NP914547.RACJZPikl6q9ea2M7Qk2hVs6MUen1UVpF-JLxkgi4l7PA130_assertion evidence source_evidence_literature NP914547.RACJZPikl6q9ea2M7Qk2hVs6MUen1UVpF-JLxkgi4l7PA130_provenance.
- NP914547.RACJZPikl6q9ea2M7Qk2hVs6MUen1UVpF-JLxkgi4l7PA130_assertion SIO_000772 18451712 NP914547.RACJZPikl6q9ea2M7Qk2hVs6MUen1UVpF-JLxkgi4l7PA130_provenance.
- NP914547.RACJZPikl6q9ea2M7Qk2hVs6MUen1UVpF-JLxkgi4l7PA130_assertion wasDerivedFrom befree-20140225 NP914547.RACJZPikl6q9ea2M7Qk2hVs6MUen1UVpF-JLxkgi4l7PA130_provenance.
- NP914547.RACJZPikl6q9ea2M7Qk2hVs6MUen1UVpF-JLxkgi4l7PA130_assertion wasGeneratedBy ECO_0000203 NP914547.RACJZPikl6q9ea2M7Qk2hVs6MUen1UVpF-JLxkgi4l7PA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP914547.RACJZPikl6q9ea2M7Qk2hVs6MUen1UVpF-JLxkgi4l7PA130_provenance.