Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP77240.RAVOwFvMnWHp6XdLjZezXDR1XDSnIccSmMb-FI8Q_ej1M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP77240.RAVOwFvMnWHp6XdLjZezXDR1XDSnIccSmMb-FI8Q_ej1M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP77240.RAVOwFvMnWHp6XdLjZezXDR1XDSnIccSmMb-FI8Q_ej1M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP77240.RAVOwFvMnWHp6XdLjZezXDR1XDSnIccSmMb-FI8Q_ej1M130_provenance.
- NP77240.RAVOwFvMnWHp6XdLjZezXDR1XDSnIccSmMb-FI8Q_ej1M130_assertion description "[We observed a frequency of 4.0% for CYP3A4*1B, not significantly different from that reported on other Caucasian European populations. CYP3A4*2 was found at an allele frequency of 4.5%, constituting the first report of the presence of this allele outside ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP77240.RAVOwFvMnWHp6XdLjZezXDR1XDSnIccSmMb-FI8Q_ej1M130_provenance.
- NP77240.RAVOwFvMnWHp6XdLjZezXDR1XDSnIccSmMb-FI8Q_ej1M130_assertion evidence source_evidence_literature NP77240.RAVOwFvMnWHp6XdLjZezXDR1XDSnIccSmMb-FI8Q_ej1M130_provenance.
- NP77240.RAVOwFvMnWHp6XdLjZezXDR1XDSnIccSmMb-FI8Q_ej1M130_assertion SIO_000772 14580164 NP77240.RAVOwFvMnWHp6XdLjZezXDR1XDSnIccSmMb-FI8Q_ej1M130_provenance.
- NP77240.RAVOwFvMnWHp6XdLjZezXDR1XDSnIccSmMb-FI8Q_ej1M130_assertion wasDerivedFrom gad-20150221 NP77240.RAVOwFvMnWHp6XdLjZezXDR1XDSnIccSmMb-FI8Q_ej1M130_provenance.
- NP77240.RAVOwFvMnWHp6XdLjZezXDR1XDSnIccSmMb-FI8Q_ej1M130_assertion wasGeneratedBy ECO_0000203 NP77240.RAVOwFvMnWHp6XdLjZezXDR1XDSnIccSmMb-FI8Q_ej1M130_provenance.
- gad-20150221 importedOn "2015-02-21" NP77240.RAVOwFvMnWHp6XdLjZezXDR1XDSnIccSmMb-FI8Q_ej1M130_provenance.