Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP382037.RAWfVWEsfl0QOaK2BiET322nwWGFnjsIpPxibs_gJVIlY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP382037.RAWfVWEsfl0QOaK2BiET322nwWGFnjsIpPxibs_gJVIlY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP382037.RAWfVWEsfl0QOaK2BiET322nwWGFnjsIpPxibs_gJVIlY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP382037.RAWfVWEsfl0QOaK2BiET322nwWGFnjsIpPxibs_gJVIlY130_provenance.
- NP382037.RAWfVWEsfl0QOaK2BiET322nwWGFnjsIpPxibs_gJVIlY130_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." NP382037.RAWfVWEsfl0QOaK2BiET322nwWGFnjsIpPxibs_gJVIlY130_provenance.
- NP382037.RAWfVWEsfl0QOaK2BiET322nwWGFnjsIpPxibs_gJVIlY130_assertion evidence source_evidence_literature NP382037.RAWfVWEsfl0QOaK2BiET322nwWGFnjsIpPxibs_gJVIlY130_provenance.
- NP382037.RAWfVWEsfl0QOaK2BiET322nwWGFnjsIpPxibs_gJVIlY130_assertion SIO_000772 20429839 NP382037.RAWfVWEsfl0QOaK2BiET322nwWGFnjsIpPxibs_gJVIlY130_provenance.
- NP382037.RAWfVWEsfl0QOaK2BiET322nwWGFnjsIpPxibs_gJVIlY130_assertion wasDerivedFrom befree-20150227 NP382037.RAWfVWEsfl0QOaK2BiET322nwWGFnjsIpPxibs_gJVIlY130_provenance.
- NP382037.RAWfVWEsfl0QOaK2BiET322nwWGFnjsIpPxibs_gJVIlY130_assertion wasGeneratedBy ECO_0000203 NP382037.RAWfVWEsfl0QOaK2BiET322nwWGFnjsIpPxibs_gJVIlY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP382037.RAWfVWEsfl0QOaK2BiET322nwWGFnjsIpPxibs_gJVIlY130_provenance.