Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP415633.RAUutHKIAszv6N8f1BxjUNLgxsozGAfEqpACBIWYo99GA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP415633.RAUutHKIAszv6N8f1BxjUNLgxsozGAfEqpACBIWYo99GA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP415633.RAUutHKIAszv6N8f1BxjUNLgxsozGAfEqpACBIWYo99GA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP415633.RAUutHKIAszv6N8f1BxjUNLgxsozGAfEqpACBIWYo99GA130_provenance.
- NP415633.RAUutHKIAszv6N8f1BxjUNLgxsozGAfEqpACBIWYo99GA130_assertion description "[The aims of this study are to investigate the most common molecular mutations of the G6PD gene among Jordanians in northern Jordan and to examine the correlation between the genotype and phenotype of this enzyme deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP415633.RAUutHKIAszv6N8f1BxjUNLgxsozGAfEqpACBIWYo99GA130_provenance.
- NP415633.RAUutHKIAszv6N8f1BxjUNLgxsozGAfEqpACBIWYo99GA130_assertion evidence source_evidence_literature NP415633.RAUutHKIAszv6N8f1BxjUNLgxsozGAfEqpACBIWYo99GA130_provenance.
- NP415633.RAUutHKIAszv6N8f1BxjUNLgxsozGAfEqpACBIWYo99GA130_assertion SIO_000772 22906837 NP415633.RAUutHKIAszv6N8f1BxjUNLgxsozGAfEqpACBIWYo99GA130_provenance.
- NP415633.RAUutHKIAszv6N8f1BxjUNLgxsozGAfEqpACBIWYo99GA130_assertion wasDerivedFrom befree-20150227 NP415633.RAUutHKIAszv6N8f1BxjUNLgxsozGAfEqpACBIWYo99GA130_provenance.
- NP415633.RAUutHKIAszv6N8f1BxjUNLgxsozGAfEqpACBIWYo99GA130_assertion wasGeneratedBy ECO_0000203 NP415633.RAUutHKIAszv6N8f1BxjUNLgxsozGAfEqpACBIWYo99GA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP415633.RAUutHKIAszv6N8f1BxjUNLgxsozGAfEqpACBIWYo99GA130_provenance.