Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP342408.RADA7WIw_WO7ZSfmS8tqXof-WQc_iEz2FM_Q5WsFC8Vjc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP342408.RADA7WIw_WO7ZSfmS8tqXof-WQc_iEz2FM_Q5WsFC8Vjc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP342408.RADA7WIw_WO7ZSfmS8tqXof-WQc_iEz2FM_Q5WsFC8Vjc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP342408.RADA7WIw_WO7ZSfmS8tqXof-WQc_iEz2FM_Q5WsFC8Vjc130_provenance.
- NP342408.RADA7WIw_WO7ZSfmS8tqXof-WQc_iEz2FM_Q5WsFC8Vjc130_assertion description "[When the CYP1A1 Val/Val and CYP2D6 HEM genotypes were taken together, the risk for SCLC was four-fold.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP342408.RADA7WIw_WO7ZSfmS8tqXof-WQc_iEz2FM_Q5WsFC8Vjc130_provenance.
- NP342408.RADA7WIw_WO7ZSfmS8tqXof-WQc_iEz2FM_Q5WsFC8Vjc130_assertion evidence source_evidence_literature NP342408.RADA7WIw_WO7ZSfmS8tqXof-WQc_iEz2FM_Q5WsFC8Vjc130_provenance.
- NP342408.RADA7WIw_WO7ZSfmS8tqXof-WQc_iEz2FM_Q5WsFC8Vjc130_assertion SIO_000772 14602525 NP342408.RADA7WIw_WO7ZSfmS8tqXof-WQc_iEz2FM_Q5WsFC8Vjc130_provenance.
- NP342408.RADA7WIw_WO7ZSfmS8tqXof-WQc_iEz2FM_Q5WsFC8Vjc130_assertion wasDerivedFrom befree-20150227 NP342408.RADA7WIw_WO7ZSfmS8tqXof-WQc_iEz2FM_Q5WsFC8Vjc130_provenance.
- NP342408.RADA7WIw_WO7ZSfmS8tqXof-WQc_iEz2FM_Q5WsFC8Vjc130_assertion wasGeneratedBy ECO_0000203 NP342408.RADA7WIw_WO7ZSfmS8tqXof-WQc_iEz2FM_Q5WsFC8Vjc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP342408.RADA7WIw_WO7ZSfmS8tqXof-WQc_iEz2FM_Q5WsFC8Vjc130_provenance.