Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP76465.RATZtMmTzvUII0gAg8aOrVw1iwDQUmX7PhmZ8XvrZ4ThY130_assertion> ?p ?o ?g. }
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- NP76465.RATZtMmTzvUII0gAg8aOrVw1iwDQUmX7PhmZ8XvrZ4ThY130_assertion type Assertion NP76465.RATZtMmTzvUII0gAg8aOrVw1iwDQUmX7PhmZ8XvrZ4ThY130_head.
- NP76465.RATZtMmTzvUII0gAg8aOrVw1iwDQUmX7PhmZ8XvrZ4ThY130_assertion description "[Because single nucleotide polymorphisms (SNPs) are the most subtle genetic variation in the genome, to examine these hypotheses, we have genotyped 30 SNPs in all five NHEJ genes (Ku70, Ku80, DNA-PKcs, Ligase IV, and XRCC4) in 254 primary breast cancer patients and 379 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP76465.RATZtMmTzvUII0gAg8aOrVw1iwDQUmX7PhmZ8XvrZ4ThY130_provenance.
- NP76465.RATZtMmTzvUII0gAg8aOrVw1iwDQUmX7PhmZ8XvrZ4ThY130_assertion evidence source_evidence_literature NP76465.RATZtMmTzvUII0gAg8aOrVw1iwDQUmX7PhmZ8XvrZ4ThY130_provenance.
- NP76465.RATZtMmTzvUII0gAg8aOrVw1iwDQUmX7PhmZ8XvrZ4ThY130_assertion SIO_000772 12750264 NP76465.RATZtMmTzvUII0gAg8aOrVw1iwDQUmX7PhmZ8XvrZ4ThY130_provenance.
- NP76465.RATZtMmTzvUII0gAg8aOrVw1iwDQUmX7PhmZ8XvrZ4ThY130_assertion wasDerivedFrom gad-20150221 NP76465.RATZtMmTzvUII0gAg8aOrVw1iwDQUmX7PhmZ8XvrZ4ThY130_provenance.
- NP76465.RATZtMmTzvUII0gAg8aOrVw1iwDQUmX7PhmZ8XvrZ4ThY130_assertion wasGeneratedBy ECO_0000203 NP76465.RATZtMmTzvUII0gAg8aOrVw1iwDQUmX7PhmZ8XvrZ4ThY130_provenance.