Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615473.RAh3WrezOxyncU_G0zXV0EweuBmTC8EzyWCMNUqEnNACk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615473.RAh3WrezOxyncU_G0zXV0EweuBmTC8EzyWCMNUqEnNACk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615473.RAh3WrezOxyncU_G0zXV0EweuBmTC8EzyWCMNUqEnNACk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615473.RAh3WrezOxyncU_G0zXV0EweuBmTC8EzyWCMNUqEnNACk130_provenance.
- NP615473.RAh3WrezOxyncU_G0zXV0EweuBmTC8EzyWCMNUqEnNACk130_assertion description "[Four controls and five patients presented three of four mutant alleles in H6PD R453Q and HSD11B1 83557insA, which is the genotype observed in some subjects with CRD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615473.RAh3WrezOxyncU_G0zXV0EweuBmTC8EzyWCMNUqEnNACk130_provenance.
- NP615473.RAh3WrezOxyncU_G0zXV0EweuBmTC8EzyWCMNUqEnNACk130_assertion evidence source_evidence_literature NP615473.RAh3WrezOxyncU_G0zXV0EweuBmTC8EzyWCMNUqEnNACk130_provenance.
- NP615473.RAh3WrezOxyncU_G0zXV0EweuBmTC8EzyWCMNUqEnNACk130_assertion SIO_000772 15827106 NP615473.RAh3WrezOxyncU_G0zXV0EweuBmTC8EzyWCMNUqEnNACk130_provenance.
- NP615473.RAh3WrezOxyncU_G0zXV0EweuBmTC8EzyWCMNUqEnNACk130_assertion wasDerivedFrom befree-20140225 NP615473.RAh3WrezOxyncU_G0zXV0EweuBmTC8EzyWCMNUqEnNACk130_provenance.
- NP615473.RAh3WrezOxyncU_G0zXV0EweuBmTC8EzyWCMNUqEnNACk130_assertion wasGeneratedBy ECO_0000203 NP615473.RAh3WrezOxyncU_G0zXV0EweuBmTC8EzyWCMNUqEnNACk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615473.RAh3WrezOxyncU_G0zXV0EweuBmTC8EzyWCMNUqEnNACk130_provenance.