Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP780037.RAjTc_EdbNSRI6J9OGb6c9t6K4U4gTvQ6Dksz-SwnNol4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP780037.RAjTc_EdbNSRI6J9OGb6c9t6K4U4gTvQ6Dksz-SwnNol4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP780037.RAjTc_EdbNSRI6J9OGb6c9t6K4U4gTvQ6Dksz-SwnNol4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP780037.RAjTc_EdbNSRI6J9OGb6c9t6K4U4gTvQ6Dksz-SwnNol4130_provenance.
- NP780037.RAjTc_EdbNSRI6J9OGb6c9t6K4U4gTvQ6Dksz-SwnNol4130_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." NP780037.RAjTc_EdbNSRI6J9OGb6c9t6K4U4gTvQ6Dksz-SwnNol4130_provenance.
- NP780037.RAjTc_EdbNSRI6J9OGb6c9t6K4U4gTvQ6Dksz-SwnNol4130_assertion evidence source_evidence_literature NP780037.RAjTc_EdbNSRI6J9OGb6c9t6K4U4gTvQ6Dksz-SwnNol4130_provenance.
- NP780037.RAjTc_EdbNSRI6J9OGb6c9t6K4U4gTvQ6Dksz-SwnNol4130_assertion SIO_000772 20429839 NP780037.RAjTc_EdbNSRI6J9OGb6c9t6K4U4gTvQ6Dksz-SwnNol4130_provenance.
- NP780037.RAjTc_EdbNSRI6J9OGb6c9t6K4U4gTvQ6Dksz-SwnNol4130_assertion wasDerivedFrom befree-20150227 NP780037.RAjTc_EdbNSRI6J9OGb6c9t6K4U4gTvQ6Dksz-SwnNol4130_provenance.
- NP780037.RAjTc_EdbNSRI6J9OGb6c9t6K4U4gTvQ6Dksz-SwnNol4130_assertion wasGeneratedBy ECO_0000203 NP780037.RAjTc_EdbNSRI6J9OGb6c9t6K4U4gTvQ6Dksz-SwnNol4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP780037.RAjTc_EdbNSRI6J9OGb6c9t6K4U4gTvQ6Dksz-SwnNol4130_provenance.