Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP328057.RAastry22wcFzEIeGChckYtOf6a1QI88SqQn-mQf0dfzQ130_assertion> ?p ?o ?g. }
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- NP328057.RAastry22wcFzEIeGChckYtOf6a1QI88SqQn-mQf0dfzQ130_assertion type Assertion NP328057.RAastry22wcFzEIeGChckYtOf6a1QI88SqQn-mQf0dfzQ130_head.
- 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.