Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP691277.RAzDKqPhkVIXmh1MJUj-DL7D9V3bhGujb0QGkKTJzAMso130_assertion> ?p ?o ?g. }
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- NP691277.RAzDKqPhkVIXmh1MJUj-DL7D9V3bhGujb0QGkKTJzAMso130_assertion type Assertion NP691277.RAzDKqPhkVIXmh1MJUj-DL7D9V3bhGujb0QGkKTJzAMso130_head.
- NP691277.RAzDKqPhkVIXmh1MJUj-DL7D9V3bhGujb0QGkKTJzAMso130_assertion description "[Moreover, we investigated the association between 5 single nucleotide polymorphisms (SNPs) in the homologous recombination DNA repair pathway (XRCC3 c.-1843 A>G, XRCC3 c.562-14 A>G, XRCC3 c.722 C>T, Rad51 c.-3429 G>C, Rad51 c.-3392 G>T) and 4 SNPs in the non- homologous end joining DNA repair pathway (Lig4 c.26 C>T, Lig4 c.1704 T>C, Ku70 c.-1310 C>G and Ku80 c.2110-2408 G>A) on one hand and the risk of the development of HNSCC on the other hand in a case- control setting in a Caucasian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691277.RAzDKqPhkVIXmh1MJUj-DL7D9V3bhGujb0QGkKTJzAMso130_provenance.
- NP691277.RAzDKqPhkVIXmh1MJUj-DL7D9V3bhGujb0QGkKTJzAMso130_assertion evidence source_evidence_literature NP691277.RAzDKqPhkVIXmh1MJUj-DL7D9V3bhGujb0QGkKTJzAMso130_provenance.
- NP691277.RAzDKqPhkVIXmh1MJUj-DL7D9V3bhGujb0QGkKTJzAMso130_assertion SIO_000772 18768166 NP691277.RAzDKqPhkVIXmh1MJUj-DL7D9V3bhGujb0QGkKTJzAMso130_provenance.
- NP691277.RAzDKqPhkVIXmh1MJUj-DL7D9V3bhGujb0QGkKTJzAMso130_assertion wasDerivedFrom befree-2016 NP691277.RAzDKqPhkVIXmh1MJUj-DL7D9V3bhGujb0QGkKTJzAMso130_provenance.
- NP691277.RAzDKqPhkVIXmh1MJUj-DL7D9V3bhGujb0QGkKTJzAMso130_assertion wasGeneratedBy ECO_0000203 NP691277.RAzDKqPhkVIXmh1MJUj-DL7D9V3bhGujb0QGkKTJzAMso130_provenance.