Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP79781.RAH0ffWYmZMtCn-KnJKnKKnjd9htqB1gEDxHkimrdDrKI130_assertion> ?p ?o ?g. }
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- NP79781.RAH0ffWYmZMtCn-KnJKnKKnjd9htqB1gEDxHkimrdDrKI130_assertion type Assertion NP79781.RAH0ffWYmZMtCn-KnJKnKKnjd9htqB1gEDxHkimrdDrKI130_head.
- NP79781.RAH0ffWYmZMtCn-KnJKnKKnjd9htqB1gEDxHkimrdDrKI130_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." NP79781.RAH0ffWYmZMtCn-KnJKnKKnjd9htqB1gEDxHkimrdDrKI130_provenance.
- NP79781.RAH0ffWYmZMtCn-KnJKnKKnjd9htqB1gEDxHkimrdDrKI130_assertion evidence source_evidence_literature NP79781.RAH0ffWYmZMtCn-KnJKnKKnjd9htqB1gEDxHkimrdDrKI130_provenance.
- NP79781.RAH0ffWYmZMtCn-KnJKnKKnjd9htqB1gEDxHkimrdDrKI130_assertion SIO_000772 12750264 NP79781.RAH0ffWYmZMtCn-KnJKnKKnjd9htqB1gEDxHkimrdDrKI130_provenance.
- NP79781.RAH0ffWYmZMtCn-KnJKnKKnjd9htqB1gEDxHkimrdDrKI130_assertion wasDerivedFrom gad-20150221 NP79781.RAH0ffWYmZMtCn-KnJKnKKnjd9htqB1gEDxHkimrdDrKI130_provenance.
- NP79781.RAH0ffWYmZMtCn-KnJKnKKnjd9htqB1gEDxHkimrdDrKI130_assertion wasGeneratedBy ECO_0000203 NP79781.RAH0ffWYmZMtCn-KnJKnKKnjd9htqB1gEDxHkimrdDrKI130_provenance.