Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP88949.RA_GH-RwKmCBmJSVRBL8PuDGP2Ls6vzFVk7PKU_nwmYjc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP88949.RA_GH-RwKmCBmJSVRBL8PuDGP2Ls6vzFVk7PKU_nwmYjc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP88949.RA_GH-RwKmCBmJSVRBL8PuDGP2Ls6vzFVk7PKU_nwmYjc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP88949.RA_GH-RwKmCBmJSVRBL8PuDGP2Ls6vzFVk7PKU_nwmYjc130_provenance.
- NP88949.RA_GH-RwKmCBmJSVRBL8PuDGP2Ls6vzFVk7PKU_nwmYjc130_assertion description "[The birth prevalence of MCADD and positive predictive value of the screening test were similar to those identified by other newborn screening programs internationally. We observed some evidence of correlation between genotype and biochemical phenotype (C8]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP88949.RA_GH-RwKmCBmJSVRBL8PuDGP2Ls6vzFVk7PKU_nwmYjc130_provenance.
- NP88949.RA_GH-RwKmCBmJSVRBL8PuDGP2Ls6vzFVk7PKU_nwmYjc130_assertion evidence source_evidence_literature NP88949.RA_GH-RwKmCBmJSVRBL8PuDGP2Ls6vzFVk7PKU_nwmYjc130_provenance.
- NP88949.RA_GH-RwKmCBmJSVRBL8PuDGP2Ls6vzFVk7PKU_nwmYjc130_assertion SIO_000772 21083904 NP88949.RA_GH-RwKmCBmJSVRBL8PuDGP2Ls6vzFVk7PKU_nwmYjc130_provenance.
- NP88949.RA_GH-RwKmCBmJSVRBL8PuDGP2Ls6vzFVk7PKU_nwmYjc130_assertion wasDerivedFrom gad-20150221 NP88949.RA_GH-RwKmCBmJSVRBL8PuDGP2Ls6vzFVk7PKU_nwmYjc130_provenance.
- NP88949.RA_GH-RwKmCBmJSVRBL8PuDGP2Ls6vzFVk7PKU_nwmYjc130_assertion wasGeneratedBy ECO_0000203 NP88949.RA_GH-RwKmCBmJSVRBL8PuDGP2Ls6vzFVk7PKU_nwmYjc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP88949.RA_GH-RwKmCBmJSVRBL8PuDGP2Ls6vzFVk7PKU_nwmYjc130_provenance.