Matches in Nanopublications for { ?s ?p "[Two rare variants (OGG1 c.137G>A; MUTYH c.1187G>A) and one common polymorphism (NUDT1 c.426C>T) were associated with CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP875484.RABPiz7FCOphVnVjMol2Av3Gq9QbgDq01B_aYSwFlVQHE130_assertion description "[Two rare variants (OGG1 c.137G>A; MUTYH c.1187G>A) and one common polymorphism (NUDT1 c.426C>T) were associated with CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP875484.RABPiz7FCOphVnVjMol2Av3Gq9QbgDq01B_aYSwFlVQHE130_provenance.
- NP574247.RA9UliJoRij-wUkhyb_wZY9VneZ1XTHHqdjopQeq5M7Rc130_assertion description "[Two rare variants (OGG1 c.137G>A; MUTYH c.1187G>A) and one common polymorphism (NUDT1 c.426C>T) were associated with CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP574247.RA9UliJoRij-wUkhyb_wZY9VneZ1XTHHqdjopQeq5M7Rc130_provenance.
- NP574226.RAYWF-5bzPeNAaD9AFZfQVIlB-w9Yc7CivZNjS77Nn1XY130_assertion description "[Two rare variants (OGG1 c.137G>A; MUTYH c.1187G>A) and one common polymorphism (NUDT1 c.426C>T) were associated with CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP574226.RAYWF-5bzPeNAaD9AFZfQVIlB-w9Yc7CivZNjS77Nn1XY130_provenance.
- NP875485.RA0Ne81dKzhI0C_rNeKkNnVn7-rxWqGYUE5WnqbX2obrk130_assertion description "[Two rare variants (OGG1 c.137G>A; MUTYH c.1187G>A) and one common polymorphism (NUDT1 c.426C>T) were associated with CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP875485.RA0Ne81dKzhI0C_rNeKkNnVn7-rxWqGYUE5WnqbX2obrk130_provenance.
- NP875489.RA8-7_CYI-6VabXrJOJlHq58Vs3x9dJeN1eOgu8rVeQz8130_assertion description "[Two rare variants (OGG1 c.137G>A; MUTYH c.1187G>A) and one common polymorphism (NUDT1 c.426C>T) were associated with CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP875489.RA8-7_CYI-6VabXrJOJlHq58Vs3x9dJeN1eOgu8rVeQz8130_provenance.
- assertion description "[Two rare variants (OGG1 c.137G>A; MUTYH c.1187G>A) and one common polymorphism (NUDT1 c.426C>T) were associated with CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Two rare variants (OGG1 c.137G>A; MUTYH c.1187G>A) and one common polymorphism (NUDT1 c.426C>T) were associated with CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Two rare variants (OGG1 c.137G>A; MUTYH c.1187G>A) and one common polymorphism (NUDT1 c.426C>T) were associated with CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP602059.RAJZCy5Yf4Ml4U35FPxqaZ3Oe5HaRy2KZdzS_VfTFNSjw130_assertion description "[Two rare variants (OGG1 c.137G>A; MUTYH c.1187G>A) and one common polymorphism (NUDT1 c.426C>T) were associated with CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP602059.RAJZCy5Yf4Ml4U35FPxqaZ3Oe5HaRy2KZdzS_VfTFNSjw130_provenance.
- assertion description "[Two rare variants (OGG1 c.137G>A; MUTYH c.1187G>A) and one common polymorphism (NUDT1 c.426C>T) were associated with CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Two rare variants (OGG1 c.137G>A; MUTYH c.1187G>A) and one common polymorphism (NUDT1 c.426C>T) were associated with CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Two rare variants (OGG1 c.137G>A; MUTYH c.1187G>A) and one common polymorphism (NUDT1 c.426C>T) were associated with CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP602381.RAvWo3ifV7h5GrOO40W-1h7zvj6vbBFQ94mkUqpTe3lvk130_assertion description "[Two rare variants (OGG1 c.137G>A; MUTYH c.1187G>A) and one common polymorphism (NUDT1 c.426C>T) were associated with CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP602381.RAvWo3ifV7h5GrOO40W-1h7zvj6vbBFQ94mkUqpTe3lvk130_provenance.
- NP875483.RAKHrkUG3JdcqO0pf1IpX1Rvl9vr_qkv0DZC1UVdjl1wY130_assertion description "[Two rare variants (OGG1 c.137G>A; MUTYH c.1187G>A) and one common polymorphism (NUDT1 c.426C>T) were associated with CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP875483.RAKHrkUG3JdcqO0pf1IpX1Rvl9vr_qkv0DZC1UVdjl1wY130_provenance.
- NP875488.RAN-7h-OFPZhpys0r9uwVP6TJC3JonkzWFwTBttws5Evk130_assertion description "[Two rare variants (OGG1 c.137G>A; MUTYH c.1187G>A) and one common polymorphism (NUDT1 c.426C>T) were associated with CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP875488.RAN-7h-OFPZhpys0r9uwVP6TJC3JonkzWFwTBttws5Evk130_provenance.
- NP875482.RAp8N9F2i8c_7Vl0eZ0TBVpNnjRcUw-djU5xcrJ3VTm70130_assertion description "[Two rare variants (OGG1 c.137G>A; MUTYH c.1187G>A) and one common polymorphism (NUDT1 c.426C>T) were associated with CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP875482.RAp8N9F2i8c_7Vl0eZ0TBVpNnjRcUw-djU5xcrJ3VTm70130_provenance.