Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP328052.RAZTw3SNadj3zN8EIjbSMsnFt9wwnpfvWVrOi-etd5utU130_assertion> ?p ?o ?g. }
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- NP328052.RAZTw3SNadj3zN8EIjbSMsnFt9wwnpfvWVrOi-etd5utU130_assertion type Assertion NP328052.RAZTw3SNadj3zN8EIjbSMsnFt9wwnpfvWVrOi-etd5utU130_head.
- NP328052.RAZTw3SNadj3zN8EIjbSMsnFt9wwnpfvWVrOi-etd5utU130_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." NP328052.RAZTw3SNadj3zN8EIjbSMsnFt9wwnpfvWVrOi-etd5utU130_provenance.
- NP328052.RAZTw3SNadj3zN8EIjbSMsnFt9wwnpfvWVrOi-etd5utU130_assertion evidence source_evidence_literature NP328052.RAZTw3SNadj3zN8EIjbSMsnFt9wwnpfvWVrOi-etd5utU130_provenance.
- NP328052.RAZTw3SNadj3zN8EIjbSMsnFt9wwnpfvWVrOi-etd5utU130_assertion SIO_000772 11520764 NP328052.RAZTw3SNadj3zN8EIjbSMsnFt9wwnpfvWVrOi-etd5utU130_provenance.
- NP328052.RAZTw3SNadj3zN8EIjbSMsnFt9wwnpfvWVrOi-etd5utU130_assertion wasDerivedFrom befree-2016 NP328052.RAZTw3SNadj3zN8EIjbSMsnFt9wwnpfvWVrOi-etd5utU130_provenance.
- NP328052.RAZTw3SNadj3zN8EIjbSMsnFt9wwnpfvWVrOi-etd5utU130_assertion wasGeneratedBy ECO_0000203 NP328052.RAZTw3SNadj3zN8EIjbSMsnFt9wwnpfvWVrOi-etd5utU130_provenance.