Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP694720.RASFJ_J6bT1JTHXsyss8W2Jf_b2e5Yrhv1ONoMypYMnhg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP694720.RASFJ_J6bT1JTHXsyss8W2Jf_b2e5Yrhv1ONoMypYMnhg130_assertion type Assertion NP694720.RASFJ_J6bT1JTHXsyss8W2Jf_b2e5Yrhv1ONoMypYMnhg130_head.
- 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.