Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP606229.RATEniGvFkXupPELy0IeNyqHptwHklXX12s5Lhl-ac9tU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP606229.RATEniGvFkXupPELy0IeNyqHptwHklXX12s5Lhl-ac9tU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP606229.RATEniGvFkXupPELy0IeNyqHptwHklXX12s5Lhl-ac9tU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP606229.RATEniGvFkXupPELy0IeNyqHptwHklXX12s5Lhl-ac9tU130_provenance.
- NP606229.RATEniGvFkXupPELy0IeNyqHptwHklXX12s5Lhl-ac9tU130_assertion description "[Severe molecular defects of a novel FOXC1 W152G mutation result in aniridia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606229.RATEniGvFkXupPELy0IeNyqHptwHklXX12s5Lhl-ac9tU130_provenance.
- NP606229.RATEniGvFkXupPELy0IeNyqHptwHklXX12s5Lhl-ac9tU130_assertion evidence source_evidence_literature NP606229.RATEniGvFkXupPELy0IeNyqHptwHklXX12s5Lhl-ac9tU130_provenance.
- NP606229.RATEniGvFkXupPELy0IeNyqHptwHklXX12s5Lhl-ac9tU130_assertion SIO_000772 19279310 NP606229.RATEniGvFkXupPELy0IeNyqHptwHklXX12s5Lhl-ac9tU130_provenance.
- NP606229.RATEniGvFkXupPELy0IeNyqHptwHklXX12s5Lhl-ac9tU130_assertion wasDerivedFrom befree-20140225 NP606229.RATEniGvFkXupPELy0IeNyqHptwHklXX12s5Lhl-ac9tU130_provenance.
- NP606229.RATEniGvFkXupPELy0IeNyqHptwHklXX12s5Lhl-ac9tU130_assertion wasGeneratedBy ECO_0000203 NP606229.RATEniGvFkXupPELy0IeNyqHptwHklXX12s5Lhl-ac9tU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP606229.RATEniGvFkXupPELy0IeNyqHptwHklXX12s5Lhl-ac9tU130_provenance.