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- NP415836.RAvXA0_ZPJjekNXoBox7yufH60lbjs3wtvSCGauqnoy1o130_assertion type Assertion NP415836.RAvXA0_ZPJjekNXoBox7yufH60lbjs3wtvSCGauqnoy1o130_head.
- NP415836.RAvXA0_ZPJjekNXoBox7yufH60lbjs3wtvSCGauqnoy1o130_assertion wasGeneratedBy ECO_0000203 NP415836.RAvXA0_ZPJjekNXoBox7yufH60lbjs3wtvSCGauqnoy1o130_provenance.
- NP415836.RAvXA0_ZPJjekNXoBox7yufH60lbjs3wtvSCGauqnoy1o130_assertion wasDerivedFrom befree-20150227 NP415836.RAvXA0_ZPJjekNXoBox7yufH60lbjs3wtvSCGauqnoy1o130_provenance.
- NP415836.RAvXA0_ZPJjekNXoBox7yufH60lbjs3wtvSCGauqnoy1o130_assertion SIO_000772 10834514 NP415836.RAvXA0_ZPJjekNXoBox7yufH60lbjs3wtvSCGauqnoy1o130_provenance.
- NP415836.RAvXA0_ZPJjekNXoBox7yufH60lbjs3wtvSCGauqnoy1o130_assertion evidence source_evidence_literature NP415836.RAvXA0_ZPJjekNXoBox7yufH60lbjs3wtvSCGauqnoy1o130_provenance.
- NP415836.RAvXA0_ZPJjekNXoBox7yufH60lbjs3wtvSCGauqnoy1o130_assertion description "[Investigation of patients with GSD I shows that those with GSD Ia are mutated in the glucose-6-phosphate hydrolase gene, whereas those diagnosed as GSD Ib, GSD Ic or GSD Id are mutated in the glucose-6-phosphate translocase gene, and are therefore GSD Ib patients, in agreement with the fact that they all have neutropenia or neutrophil dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP415836.RAvXA0_ZPJjekNXoBox7yufH60lbjs3wtvSCGauqnoy1o130_provenance.