Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP750361.RA8Vz8rLVA_G3hqBoNBJer6RaN0gIbjxU293owoDFQ2ow130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP750361.RA8Vz8rLVA_G3hqBoNBJer6RaN0gIbjxU293owoDFQ2ow130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP750361.RA8Vz8rLVA_G3hqBoNBJer6RaN0gIbjxU293owoDFQ2ow130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP750361.RA8Vz8rLVA_G3hqBoNBJer6RaN0gIbjxU293owoDFQ2ow130_provenance.
- NP750361.RA8Vz8rLVA_G3hqBoNBJer6RaN0gIbjxU293owoDFQ2ow130_assertion description "[Marginally statistically significant association was found for XRCC1 codon 399 (for Caucasians only), XPD Asp312Asn and XRCC1 codon 194 variants and head and neck cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP750361.RA8Vz8rLVA_G3hqBoNBJer6RaN0gIbjxU293owoDFQ2ow130_provenance.
- NP750361.RA8Vz8rLVA_G3hqBoNBJer6RaN0gIbjxU293owoDFQ2ow130_assertion evidence source_evidence_literature NP750361.RA8Vz8rLVA_G3hqBoNBJer6RaN0gIbjxU293owoDFQ2ow130_provenance.
- NP750361.RA8Vz8rLVA_G3hqBoNBJer6RaN0gIbjxU293owoDFQ2ow130_assertion SIO_000772 20429839 NP750361.RA8Vz8rLVA_G3hqBoNBJer6RaN0gIbjxU293owoDFQ2ow130_provenance.
- NP750361.RA8Vz8rLVA_G3hqBoNBJer6RaN0gIbjxU293owoDFQ2ow130_assertion wasDerivedFrom befree-20140225 NP750361.RA8Vz8rLVA_G3hqBoNBJer6RaN0gIbjxU293owoDFQ2ow130_provenance.
- NP750361.RA8Vz8rLVA_G3hqBoNBJer6RaN0gIbjxU293owoDFQ2ow130_assertion wasGeneratedBy ECO_0000203 NP750361.RA8Vz8rLVA_G3hqBoNBJer6RaN0gIbjxU293owoDFQ2ow130_provenance.
- befree-20140225 importedOn "2014-02-25" NP750361.RA8Vz8rLVA_G3hqBoNBJer6RaN0gIbjxU293owoDFQ2ow130_provenance.