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- source_evidence_literature type ECO_0000212 NP694720.RASFJ_J6bT1JTHXsyss8W2Jf_b2e5Yrhv1ONoMypYMnhg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694720.RASFJ_J6bT1JTHXsyss8W2Jf_b2e5Yrhv1ONoMypYMnhg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694720.RASFJ_J6bT1JTHXsyss8W2Jf_b2e5Yrhv1ONoMypYMnhg130_provenance.
- NP694720.RASFJ_J6bT1JTHXsyss8W2Jf_b2e5Yrhv1ONoMypYMnhg130_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." NP694720.RASFJ_J6bT1JTHXsyss8W2Jf_b2e5Yrhv1ONoMypYMnhg130_provenance.
- NP694720.RASFJ_J6bT1JTHXsyss8W2Jf_b2e5Yrhv1ONoMypYMnhg130_assertion evidence source_evidence_literature NP694720.RASFJ_J6bT1JTHXsyss8W2Jf_b2e5Yrhv1ONoMypYMnhg130_provenance.
- NP694720.RASFJ_J6bT1JTHXsyss8W2Jf_b2e5Yrhv1ONoMypYMnhg130_assertion SIO_000772 11471167 NP694720.RASFJ_J6bT1JTHXsyss8W2Jf_b2e5Yrhv1ONoMypYMnhg130_provenance.
- NP694720.RASFJ_J6bT1JTHXsyss8W2Jf_b2e5Yrhv1ONoMypYMnhg130_assertion wasDerivedFrom befree-20140225 NP694720.RASFJ_J6bT1JTHXsyss8W2Jf_b2e5Yrhv1ONoMypYMnhg130_provenance.
- NP694720.RASFJ_J6bT1JTHXsyss8W2Jf_b2e5Yrhv1ONoMypYMnhg130_assertion wasGeneratedBy ECO_0000203 NP694720.RASFJ_J6bT1JTHXsyss8W2Jf_b2e5Yrhv1ONoMypYMnhg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP694720.RASFJ_J6bT1JTHXsyss8W2Jf_b2e5Yrhv1ONoMypYMnhg130_provenance.