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- source_evidence_literature type ECO_0000212 NP328057.RAastry22wcFzEIeGChckYtOf6a1QI88SqQn-mQf0dfzQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP328057.RAastry22wcFzEIeGChckYtOf6a1QI88SqQn-mQf0dfzQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP328057.RAastry22wcFzEIeGChckYtOf6a1QI88SqQn-mQf0dfzQ130_provenance.
- NP328057.RAastry22wcFzEIeGChckYtOf6a1QI88SqQn-mQf0dfzQ130_assertion description "[The present family shows absent hypopigmentation in two patients of a white family with a deletion in the OA1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328057.RAastry22wcFzEIeGChckYtOf6a1QI88SqQn-mQf0dfzQ130_provenance.
- NP328057.RAastry22wcFzEIeGChckYtOf6a1QI88SqQn-mQf0dfzQ130_assertion evidence source_evidence_literature NP328057.RAastry22wcFzEIeGChckYtOf6a1QI88SqQn-mQf0dfzQ130_provenance.
- NP328057.RAastry22wcFzEIeGChckYtOf6a1QI88SqQn-mQf0dfzQ130_assertion SIO_000772 11520764 NP328057.RAastry22wcFzEIeGChckYtOf6a1QI88SqQn-mQf0dfzQ130_provenance.
- NP328057.RAastry22wcFzEIeGChckYtOf6a1QI88SqQn-mQf0dfzQ130_assertion wasDerivedFrom befree-2016 NP328057.RAastry22wcFzEIeGChckYtOf6a1QI88SqQn-mQf0dfzQ130_provenance.
- NP328057.RAastry22wcFzEIeGChckYtOf6a1QI88SqQn-mQf0dfzQ130_assertion wasGeneratedBy ECO_0000203 NP328057.RAastry22wcFzEIeGChckYtOf6a1QI88SqQn-mQf0dfzQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP328057.RAastry22wcFzEIeGChckYtOf6a1QI88SqQn-mQf0dfzQ130_provenance.