Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP866051.RA3oafHdj6wRFkxXeeT79MPLiZpuUVx_Pq_Y-jkvrMbsY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP866051.RA3oafHdj6wRFkxXeeT79MPLiZpuUVx_Pq_Y-jkvrMbsY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP866051.RA3oafHdj6wRFkxXeeT79MPLiZpuUVx_Pq_Y-jkvrMbsY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP866051.RA3oafHdj6wRFkxXeeT79MPLiZpuUVx_Pq_Y-jkvrMbsY130_provenance.
- NP866051.RA3oafHdj6wRFkxXeeT79MPLiZpuUVx_Pq_Y-jkvrMbsY130_assertion description "[Gp91phox is encoded on the X-chromosome and p22phox, p47phox and p67phox on different autosomal chromosomes, and a defect in one of these components leads to CGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866051.RA3oafHdj6wRFkxXeeT79MPLiZpuUVx_Pq_Y-jkvrMbsY130_provenance.
- NP866051.RA3oafHdj6wRFkxXeeT79MPLiZpuUVx_Pq_Y-jkvrMbsY130_assertion evidence source_evidence_literature NP866051.RA3oafHdj6wRFkxXeeT79MPLiZpuUVx_Pq_Y-jkvrMbsY130_provenance.
- NP866051.RA3oafHdj6wRFkxXeeT79MPLiZpuUVx_Pq_Y-jkvrMbsY130_assertion SIO_000772 9618766 NP866051.RA3oafHdj6wRFkxXeeT79MPLiZpuUVx_Pq_Y-jkvrMbsY130_provenance.
- NP866051.RA3oafHdj6wRFkxXeeT79MPLiZpuUVx_Pq_Y-jkvrMbsY130_assertion wasDerivedFrom befree-20140225 NP866051.RA3oafHdj6wRFkxXeeT79MPLiZpuUVx_Pq_Y-jkvrMbsY130_provenance.
- NP866051.RA3oafHdj6wRFkxXeeT79MPLiZpuUVx_Pq_Y-jkvrMbsY130_assertion wasGeneratedBy ECO_0000203 NP866051.RA3oafHdj6wRFkxXeeT79MPLiZpuUVx_Pq_Y-jkvrMbsY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP866051.RA3oafHdj6wRFkxXeeT79MPLiZpuUVx_Pq_Y-jkvrMbsY130_provenance.