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- source_evidence_literature type ECO_0000212 NP274268.RAp39hjE_VQjAjsreNEq6KumNccDj7O04wlPT48cx2f0Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP274268.RAp39hjE_VQjAjsreNEq6KumNccDj7O04wlPT48cx2f0Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP274268.RAp39hjE_VQjAjsreNEq6KumNccDj7O04wlPT48cx2f0Q130_provenance.
- NP274268.RAp39hjE_VQjAjsreNEq6KumNccDj7O04wlPT48cx2f0Q130_assertion description "[To report two Japanese patients who were clinically diagnosed with late-onset and sporadic lattice corneal dystrophy (LCD) in whom a Leu527Arg mutation in the TGFBI gene was found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274268.RAp39hjE_VQjAjsreNEq6KumNccDj7O04wlPT48cx2f0Q130_provenance.
- NP274268.RAp39hjE_VQjAjsreNEq6KumNccDj7O04wlPT48cx2f0Q130_assertion evidence source_evidence_literature NP274268.RAp39hjE_VQjAjsreNEq6KumNccDj7O04wlPT48cx2f0Q130_provenance.
- NP274268.RAp39hjE_VQjAjsreNEq6KumNccDj7O04wlPT48cx2f0Q130_assertion SIO_000772 11413411 NP274268.RAp39hjE_VQjAjsreNEq6KumNccDj7O04wlPT48cx2f0Q130_provenance.
- NP274268.RAp39hjE_VQjAjsreNEq6KumNccDj7O04wlPT48cx2f0Q130_assertion wasDerivedFrom befree-20140225 NP274268.RAp39hjE_VQjAjsreNEq6KumNccDj7O04wlPT48cx2f0Q130_provenance.
- NP274268.RAp39hjE_VQjAjsreNEq6KumNccDj7O04wlPT48cx2f0Q130_assertion wasGeneratedBy ECO_0000203 NP274268.RAp39hjE_VQjAjsreNEq6KumNccDj7O04wlPT48cx2f0Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP274268.RAp39hjE_VQjAjsreNEq6KumNccDj7O04wlPT48cx2f0Q130_provenance.