Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP586638.RABctqYh_9HwKKVofbK9vCYGoZhAeJyCWWrMjJ_sHfcis130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP586638.RABctqYh_9HwKKVofbK9vCYGoZhAeJyCWWrMjJ_sHfcis130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP586638.RABctqYh_9HwKKVofbK9vCYGoZhAeJyCWWrMjJ_sHfcis130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP586638.RABctqYh_9HwKKVofbK9vCYGoZhAeJyCWWrMjJ_sHfcis130_provenance.
- NP586638.RABctqYh_9HwKKVofbK9vCYGoZhAeJyCWWrMjJ_sHfcis130_assertion description "[This is the first report on the studies of XPC and XRCC1 Arg194Trp polymorphisms in PC, and our present data suggest that XPC Lys939Gln and the T-A haplotype of XRCC1 Arg194Trp and Arg399Gln may be risk factors for PC in Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586638.RABctqYh_9HwKKVofbK9vCYGoZhAeJyCWWrMjJ_sHfcis130_provenance.
- NP586638.RABctqYh_9HwKKVofbK9vCYGoZhAeJyCWWrMjJ_sHfcis130_assertion evidence source_evidence_literature NP586638.RABctqYh_9HwKKVofbK9vCYGoZhAeJyCWWrMjJ_sHfcis130_provenance.
- NP586638.RABctqYh_9HwKKVofbK9vCYGoZhAeJyCWWrMjJ_sHfcis130_assertion SIO_000772 17196815 NP586638.RABctqYh_9HwKKVofbK9vCYGoZhAeJyCWWrMjJ_sHfcis130_provenance.
- NP586638.RABctqYh_9HwKKVofbK9vCYGoZhAeJyCWWrMjJ_sHfcis130_assertion wasDerivedFrom befree-2016 NP586638.RABctqYh_9HwKKVofbK9vCYGoZhAeJyCWWrMjJ_sHfcis130_provenance.
- NP586638.RABctqYh_9HwKKVofbK9vCYGoZhAeJyCWWrMjJ_sHfcis130_assertion wasGeneratedBy ECO_0000203 NP586638.RABctqYh_9HwKKVofbK9vCYGoZhAeJyCWWrMjJ_sHfcis130_provenance.
- befree-2016 importedOn "2016-02-19" NP586638.RABctqYh_9HwKKVofbK9vCYGoZhAeJyCWWrMjJ_sHfcis130_provenance.