Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP342188.RAPaa0Sy8vfqyeQ3KSEnCh1mhKXAPyzlNKReLmjXQiIU8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP342188.RAPaa0Sy8vfqyeQ3KSEnCh1mhKXAPyzlNKReLmjXQiIU8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP342188.RAPaa0Sy8vfqyeQ3KSEnCh1mhKXAPyzlNKReLmjXQiIU8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP342188.RAPaa0Sy8vfqyeQ3KSEnCh1mhKXAPyzlNKReLmjXQiIU8130_provenance.
- NP342188.RAPaa0Sy8vfqyeQ3KSEnCh1mhKXAPyzlNKReLmjXQiIU8130_assertion description "[However, in the presence of at least a single copy of the variant CYP1A1 MspI allele and the CYP2D6 HEM genotype, the risk was two-fold for squamous cell carcinoma (SQCC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP342188.RAPaa0Sy8vfqyeQ3KSEnCh1mhKXAPyzlNKReLmjXQiIU8130_provenance.
- NP342188.RAPaa0Sy8vfqyeQ3KSEnCh1mhKXAPyzlNKReLmjXQiIU8130_assertion evidence source_evidence_literature NP342188.RAPaa0Sy8vfqyeQ3KSEnCh1mhKXAPyzlNKReLmjXQiIU8130_provenance.
- NP342188.RAPaa0Sy8vfqyeQ3KSEnCh1mhKXAPyzlNKReLmjXQiIU8130_assertion SIO_000772 14602525 NP342188.RAPaa0Sy8vfqyeQ3KSEnCh1mhKXAPyzlNKReLmjXQiIU8130_provenance.
- NP342188.RAPaa0Sy8vfqyeQ3KSEnCh1mhKXAPyzlNKReLmjXQiIU8130_assertion wasDerivedFrom befree-20150227 NP342188.RAPaa0Sy8vfqyeQ3KSEnCh1mhKXAPyzlNKReLmjXQiIU8130_provenance.
- NP342188.RAPaa0Sy8vfqyeQ3KSEnCh1mhKXAPyzlNKReLmjXQiIU8130_assertion wasGeneratedBy ECO_0000203 NP342188.RAPaa0Sy8vfqyeQ3KSEnCh1mhKXAPyzlNKReLmjXQiIU8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP342188.RAPaa0Sy8vfqyeQ3KSEnCh1mhKXAPyzlNKReLmjXQiIU8130_provenance.