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- source_evidence_literature type ECO_0000212 NP236993.RAnunBTbnYLxEbarJtVCwGZywJhpkb-yucqa3W2IeG54I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP236993.RAnunBTbnYLxEbarJtVCwGZywJhpkb-yucqa3W2IeG54I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP236993.RAnunBTbnYLxEbarJtVCwGZywJhpkb-yucqa3W2IeG54I130_provenance.
- NP236993.RAnunBTbnYLxEbarJtVCwGZywJhpkb-yucqa3W2IeG54I130_assertion description "[We conclude that ALX3 is essential for normal facial development in humans and that deficiency causes a clinically recognizable phenotype, which we term frontorhiny.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP236993.RAnunBTbnYLxEbarJtVCwGZywJhpkb-yucqa3W2IeG54I130_provenance.
- NP236993.RAnunBTbnYLxEbarJtVCwGZywJhpkb-yucqa3W2IeG54I130_assertion evidence source_evidence_literature NP236993.RAnunBTbnYLxEbarJtVCwGZywJhpkb-yucqa3W2IeG54I130_provenance.
- NP236993.RAnunBTbnYLxEbarJtVCwGZywJhpkb-yucqa3W2IeG54I130_assertion SIO_000772 19409524 NP236993.RAnunBTbnYLxEbarJtVCwGZywJhpkb-yucqa3W2IeG54I130_provenance.
- NP236993.RAnunBTbnYLxEbarJtVCwGZywJhpkb-yucqa3W2IeG54I130_assertion wasDerivedFrom befree-20150227 NP236993.RAnunBTbnYLxEbarJtVCwGZywJhpkb-yucqa3W2IeG54I130_provenance.
- NP236993.RAnunBTbnYLxEbarJtVCwGZywJhpkb-yucqa3W2IeG54I130_assertion wasGeneratedBy ECO_0000203 NP236993.RAnunBTbnYLxEbarJtVCwGZywJhpkb-yucqa3W2IeG54I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP236993.RAnunBTbnYLxEbarJtVCwGZywJhpkb-yucqa3W2IeG54I130_provenance.