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- source_evidence_literature type ECO_0000212 NP368457.RANGinWZtxOLpIU7fLZ-bQLsmO902kI6ev2A5ItCkXEK4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP368457.RANGinWZtxOLpIU7fLZ-bQLsmO902kI6ev2A5ItCkXEK4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP368457.RANGinWZtxOLpIU7fLZ-bQLsmO902kI6ev2A5ItCkXEK4130_provenance.
- NP368457.RANGinWZtxOLpIU7fLZ-bQLsmO902kI6ev2A5ItCkXEK4130_assertion description "[Autosomal recessive Stargardt disease (STGD1) is a macular dystrophy caused by mutations in the ABCA4 (ABCR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP368457.RANGinWZtxOLpIU7fLZ-bQLsmO902kI6ev2A5ItCkXEK4130_provenance.
- NP368457.RANGinWZtxOLpIU7fLZ-bQLsmO902kI6ev2A5ItCkXEK4130_assertion evidence source_evidence_literature NP368457.RANGinWZtxOLpIU7fLZ-bQLsmO902kI6ev2A5ItCkXEK4130_provenance.
- NP368457.RANGinWZtxOLpIU7fLZ-bQLsmO902kI6ev2A5ItCkXEK4130_assertion SIO_000772 18463687 NP368457.RANGinWZtxOLpIU7fLZ-bQLsmO902kI6ev2A5ItCkXEK4130_provenance.
- NP368457.RANGinWZtxOLpIU7fLZ-bQLsmO902kI6ev2A5ItCkXEK4130_assertion wasDerivedFrom befree-20140225 NP368457.RANGinWZtxOLpIU7fLZ-bQLsmO902kI6ev2A5ItCkXEK4130_provenance.
- NP368457.RANGinWZtxOLpIU7fLZ-bQLsmO902kI6ev2A5ItCkXEK4130_assertion wasGeneratedBy ECO_0000203 NP368457.RANGinWZtxOLpIU7fLZ-bQLsmO902kI6ev2A5ItCkXEK4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP368457.RANGinWZtxOLpIU7fLZ-bQLsmO902kI6ev2A5ItCkXEK4130_provenance.