Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP285346.RADPWgUUM2JMa3-HAtZv_HxqtHg1Vc5UK1nEaEUEQx13U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP285346.RADPWgUUM2JMa3-HAtZv_HxqtHg1Vc5UK1nEaEUEQx13U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285346.RADPWgUUM2JMa3-HAtZv_HxqtHg1Vc5UK1nEaEUEQx13U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285346.RADPWgUUM2JMa3-HAtZv_HxqtHg1Vc5UK1nEaEUEQx13U130_provenance.
- befree-2016 importedOn "2016-02-19" NP285346.RADPWgUUM2JMa3-HAtZv_HxqtHg1Vc5UK1nEaEUEQx13U130_provenance.
- NP285346.RADPWgUUM2JMa3-HAtZv_HxqtHg1Vc5UK1nEaEUEQx13U130_assertion wasGeneratedBy ECO_0000203 NP285346.RADPWgUUM2JMa3-HAtZv_HxqtHg1Vc5UK1nEaEUEQx13U130_provenance.
- NP285346.RADPWgUUM2JMa3-HAtZv_HxqtHg1Vc5UK1nEaEUEQx13U130_assertion wasDerivedFrom befree-2016 NP285346.RADPWgUUM2JMa3-HAtZv_HxqtHg1Vc5UK1nEaEUEQx13U130_provenance.
- NP285346.RADPWgUUM2JMa3-HAtZv_HxqtHg1Vc5UK1nEaEUEQx13U130_assertion SIO_000772 10834514 NP285346.RADPWgUUM2JMa3-HAtZv_HxqtHg1Vc5UK1nEaEUEQx13U130_provenance.
- NP285346.RADPWgUUM2JMa3-HAtZv_HxqtHg1Vc5UK1nEaEUEQx13U130_assertion evidence source_evidence_literature NP285346.RADPWgUUM2JMa3-HAtZv_HxqtHg1Vc5UK1nEaEUEQx13U130_provenance.
- NP285346.RADPWgUUM2JMa3-HAtZv_HxqtHg1Vc5UK1nEaEUEQx13U130_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." NP285346.RADPWgUUM2JMa3-HAtZv_HxqtHg1Vc5UK1nEaEUEQx13U130_provenance.