Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP779829.RAfbFhFgJSxnldYooAtQsJjKZJB9Z3L-p4zVU7_CTYhQI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP779829.RAfbFhFgJSxnldYooAtQsJjKZJB9Z3L-p4zVU7_CTYhQI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP779829.RAfbFhFgJSxnldYooAtQsJjKZJB9Z3L-p4zVU7_CTYhQI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP779829.RAfbFhFgJSxnldYooAtQsJjKZJB9Z3L-p4zVU7_CTYhQI130_provenance.
- NP779829.RAfbFhFgJSxnldYooAtQsJjKZJB9Z3L-p4zVU7_CTYhQI130_assertion description "[Influence of common XPD and XRCC1 variant alleles on p53 mutations in lung tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP779829.RAfbFhFgJSxnldYooAtQsJjKZJB9Z3L-p4zVU7_CTYhQI130_provenance.
- NP779829.RAfbFhFgJSxnldYooAtQsJjKZJB9Z3L-p4zVU7_CTYhQI130_assertion evidence source_evidence_literature NP779829.RAfbFhFgJSxnldYooAtQsJjKZJB9Z3L-p4zVU7_CTYhQI130_provenance.
- NP779829.RAfbFhFgJSxnldYooAtQsJjKZJB9Z3L-p4zVU7_CTYhQI130_assertion SIO_000772 12552590 NP779829.RAfbFhFgJSxnldYooAtQsJjKZJB9Z3L-p4zVU7_CTYhQI130_provenance.
- NP779829.RAfbFhFgJSxnldYooAtQsJjKZJB9Z3L-p4zVU7_CTYhQI130_assertion wasDerivedFrom befree-20150227 NP779829.RAfbFhFgJSxnldYooAtQsJjKZJB9Z3L-p4zVU7_CTYhQI130_provenance.
- NP779829.RAfbFhFgJSxnldYooAtQsJjKZJB9Z3L-p4zVU7_CTYhQI130_assertion wasGeneratedBy ECO_0000203 NP779829.RAfbFhFgJSxnldYooAtQsJjKZJB9Z3L-p4zVU7_CTYhQI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP779829.RAfbFhFgJSxnldYooAtQsJjKZJB9Z3L-p4zVU7_CTYhQI130_provenance.