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- source_evidence_literature type ECO_0000212 NP867522.RA4ezcqkIqB5WaPeTcdv28lA78CwDVFXfMujTp36baw10130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867522.RA4ezcqkIqB5WaPeTcdv28lA78CwDVFXfMujTp36baw10130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867522.RA4ezcqkIqB5WaPeTcdv28lA78CwDVFXfMujTp36baw10130_provenance.
- NP867522.RA4ezcqkIqB5WaPeTcdv28lA78CwDVFXfMujTp36baw10130_assertion description "[We also performed a full genome screen for chromosomal abnormalities, and searched for mutations in two genes (GPR143 and OCA2) known to be associated with ocular albinism and PAX6 gene known to be associated with aniridia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867522.RA4ezcqkIqB5WaPeTcdv28lA78CwDVFXfMujTp36baw10130_provenance.
- NP867522.RA4ezcqkIqB5WaPeTcdv28lA78CwDVFXfMujTp36baw10130_assertion evidence source_evidence_literature NP867522.RA4ezcqkIqB5WaPeTcdv28lA78CwDVFXfMujTp36baw10130_provenance.
- NP867522.RA4ezcqkIqB5WaPeTcdv28lA78CwDVFXfMujTp36baw10130_assertion SIO_000772 21264491 NP867522.RA4ezcqkIqB5WaPeTcdv28lA78CwDVFXfMujTp36baw10130_provenance.
- NP867522.RA4ezcqkIqB5WaPeTcdv28lA78CwDVFXfMujTp36baw10130_assertion wasDerivedFrom befree-2016 NP867522.RA4ezcqkIqB5WaPeTcdv28lA78CwDVFXfMujTp36baw10130_provenance.
- NP867522.RA4ezcqkIqB5WaPeTcdv28lA78CwDVFXfMujTp36baw10130_assertion wasGeneratedBy ECO_0000203 NP867522.RA4ezcqkIqB5WaPeTcdv28lA78CwDVFXfMujTp36baw10130_provenance.
- befree-2016 importedOn "2016-02-19" NP867522.RA4ezcqkIqB5WaPeTcdv28lA78CwDVFXfMujTp36baw10130_provenance.