Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP340459.RAa41IGvsLA2mtC2cNHXMM-IHHofEw8WLss_Qk1EHSRf8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP340459.RAa41IGvsLA2mtC2cNHXMM-IHHofEw8WLss_Qk1EHSRf8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP340459.RAa41IGvsLA2mtC2cNHXMM-IHHofEw8WLss_Qk1EHSRf8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP340459.RAa41IGvsLA2mtC2cNHXMM-IHHofEw8WLss_Qk1EHSRf8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP340459.RAa41IGvsLA2mtC2cNHXMM-IHHofEw8WLss_Qk1EHSRf8130_provenance.
- NP340459.RAa41IGvsLA2mtC2cNHXMM-IHHofEw8WLss_Qk1EHSRf8130_assertion wasGeneratedBy ECO_0000203 NP340459.RAa41IGvsLA2mtC2cNHXMM-IHHofEw8WLss_Qk1EHSRf8130_provenance.
- NP340459.RAa41IGvsLA2mtC2cNHXMM-IHHofEw8WLss_Qk1EHSRf8130_assertion wasDerivedFrom befree-20150227 NP340459.RAa41IGvsLA2mtC2cNHXMM-IHHofEw8WLss_Qk1EHSRf8130_provenance.
- NP340459.RAa41IGvsLA2mtC2cNHXMM-IHHofEw8WLss_Qk1EHSRf8130_assertion SIO_000772 24519899 NP340459.RAa41IGvsLA2mtC2cNHXMM-IHHofEw8WLss_Qk1EHSRf8130_provenance.
- NP340459.RAa41IGvsLA2mtC2cNHXMM-IHHofEw8WLss_Qk1EHSRf8130_assertion evidence source_evidence_literature NP340459.RAa41IGvsLA2mtC2cNHXMM-IHHofEw8WLss_Qk1EHSRf8130_provenance.
- NP340459.RAa41IGvsLA2mtC2cNHXMM-IHHofEw8WLss_Qk1EHSRf8130_assertion description "[However, cases carrying haplotypes with variant alleles of both CYP1A1*2A and *2C or CYP1B1*2 and *3 or CYP2E1*5B and *6 were at significant risk of developing HNSCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP340459.RAa41IGvsLA2mtC2cNHXMM-IHHofEw8WLss_Qk1EHSRf8130_provenance.