Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP537408.RAMoxVnWZhF09r0VL71gikU-EGMH1TlWyHhVmU4EcAILs130_assertion> ?p ?o ?g. }
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- NP537408.RAMoxVnWZhF09r0VL71gikU-EGMH1TlWyHhVmU4EcAILs130_assertion type Assertion NP537408.RAMoxVnWZhF09r0VL71gikU-EGMH1TlWyHhVmU4EcAILs130_head.
- NP537408.RAMoxVnWZhF09r0VL71gikU-EGMH1TlWyHhVmU4EcAILs130_assertion description "[The data from this study show overall risk modulation of BCC by variant allele for T241M polymorphism in XRCC3 and gender-specific effect by E185Q polymorphism in NBS1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537408.RAMoxVnWZhF09r0VL71gikU-EGMH1TlWyHhVmU4EcAILs130_provenance.
- NP537408.RAMoxVnWZhF09r0VL71gikU-EGMH1TlWyHhVmU4EcAILs130_assertion evidence source_evidence_literature NP537408.RAMoxVnWZhF09r0VL71gikU-EGMH1TlWyHhVmU4EcAILs130_provenance.
- NP537408.RAMoxVnWZhF09r0VL71gikU-EGMH1TlWyHhVmU4EcAILs130_assertion SIO_000772 16501254 NP537408.RAMoxVnWZhF09r0VL71gikU-EGMH1TlWyHhVmU4EcAILs130_provenance.
- NP537408.RAMoxVnWZhF09r0VL71gikU-EGMH1TlWyHhVmU4EcAILs130_assertion wasDerivedFrom befree-2016 NP537408.RAMoxVnWZhF09r0VL71gikU-EGMH1TlWyHhVmU4EcAILs130_provenance.
- NP537408.RAMoxVnWZhF09r0VL71gikU-EGMH1TlWyHhVmU4EcAILs130_assertion wasGeneratedBy ECO_0000203 NP537408.RAMoxVnWZhF09r0VL71gikU-EGMH1TlWyHhVmU4EcAILs130_provenance.