Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP325032.RAqc3psSpuHnzWnnJi7iNYuN4oypZX9Lvz4WG0Q5v0Um0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP325032.RAqc3psSpuHnzWnnJi7iNYuN4oypZX9Lvz4WG0Q5v0Um0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP325032.RAqc3psSpuHnzWnnJi7iNYuN4oypZX9Lvz4WG0Q5v0Um0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP325032.RAqc3psSpuHnzWnnJi7iNYuN4oypZX9Lvz4WG0Q5v0Um0130_provenance.
- NP325032.RAqc3psSpuHnzWnnJi7iNYuN4oypZX9Lvz4WG0Q5v0Um0130_assertion description "[Recent studies suggest an association between the EPHX1 codon 113 polymorphism or homozygous null GSTM1 allele and the risk of carcinogenesis, emphysema, phenytoin-associated oral clefting, and the risk of spontaneous abortion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP325032.RAqc3psSpuHnzWnnJi7iNYuN4oypZX9Lvz4WG0Q5v0Um0130_provenance.
- NP325032.RAqc3psSpuHnzWnnJi7iNYuN4oypZX9Lvz4WG0Q5v0Um0130_assertion evidence source_evidence_literature NP325032.RAqc3psSpuHnzWnnJi7iNYuN4oypZX9Lvz4WG0Q5v0Um0130_provenance.
- NP325032.RAqc3psSpuHnzWnnJi7iNYuN4oypZX9Lvz4WG0Q5v0Um0130_assertion SIO_000772 11471167 NP325032.RAqc3psSpuHnzWnnJi7iNYuN4oypZX9Lvz4WG0Q5v0Um0130_provenance.
- NP325032.RAqc3psSpuHnzWnnJi7iNYuN4oypZX9Lvz4WG0Q5v0Um0130_assertion wasDerivedFrom befree-2016 NP325032.RAqc3psSpuHnzWnnJi7iNYuN4oypZX9Lvz4WG0Q5v0Um0130_provenance.
- NP325032.RAqc3psSpuHnzWnnJi7iNYuN4oypZX9Lvz4WG0Q5v0Um0130_assertion wasGeneratedBy ECO_0000203 NP325032.RAqc3psSpuHnzWnnJi7iNYuN4oypZX9Lvz4WG0Q5v0Um0130_provenance.
- befree-2016 importedOn "2016-02-19" NP325032.RAqc3psSpuHnzWnnJi7iNYuN4oypZX9Lvz4WG0Q5v0Um0130_provenance.