Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP340369.RAfz1jIfXBB_vmgein-S1GNo0F4lgau2ffsA0fCcVuw2M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP340369.RAfz1jIfXBB_vmgein-S1GNo0F4lgau2ffsA0fCcVuw2M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP340369.RAfz1jIfXBB_vmgein-S1GNo0F4lgau2ffsA0fCcVuw2M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP340369.RAfz1jIfXBB_vmgein-S1GNo0F4lgau2ffsA0fCcVuw2M130_provenance.
- NP340369.RAfz1jIfXBB_vmgein-S1GNo0F4lgau2ffsA0fCcVuw2M130_assertion description "[The GSTM1 deletion and the variant (GG) genotype of the CYP1B1 rs1800440 polymorphism were associated with a decreased risk of developing endometrial cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP340369.RAfz1jIfXBB_vmgein-S1GNo0F4lgau2ffsA0fCcVuw2M130_provenance.
- NP340369.RAfz1jIfXBB_vmgein-S1GNo0F4lgau2ffsA0fCcVuw2M130_assertion evidence source_evidence_literature NP340369.RAfz1jIfXBB_vmgein-S1GNo0F4lgau2ffsA0fCcVuw2M130_provenance.
- NP340369.RAfz1jIfXBB_vmgein-S1GNo0F4lgau2ffsA0fCcVuw2M130_assertion SIO_000772 20381444 NP340369.RAfz1jIfXBB_vmgein-S1GNo0F4lgau2ffsA0fCcVuw2M130_provenance.
- NP340369.RAfz1jIfXBB_vmgein-S1GNo0F4lgau2ffsA0fCcVuw2M130_assertion wasDerivedFrom befree-20150227 NP340369.RAfz1jIfXBB_vmgein-S1GNo0F4lgau2ffsA0fCcVuw2M130_provenance.
- NP340369.RAfz1jIfXBB_vmgein-S1GNo0F4lgau2ffsA0fCcVuw2M130_assertion wasGeneratedBy ECO_0000203 NP340369.RAfz1jIfXBB_vmgein-S1GNo0F4lgau2ffsA0fCcVuw2M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP340369.RAfz1jIfXBB_vmgein-S1GNo0F4lgau2ffsA0fCcVuw2M130_provenance.