Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP558791.RAQrx-eIgApE1XHzQV6JXiLDdTEgZiZn0nVtUJxCPm6GY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP558791.RAQrx-eIgApE1XHzQV6JXiLDdTEgZiZn0nVtUJxCPm6GY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP558791.RAQrx-eIgApE1XHzQV6JXiLDdTEgZiZn0nVtUJxCPm6GY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP558791.RAQrx-eIgApE1XHzQV6JXiLDdTEgZiZn0nVtUJxCPm6GY130_provenance.
- NP558791.RAQrx-eIgApE1XHzQV6JXiLDdTEgZiZn0nVtUJxCPm6GY130_assertion wasGeneratedBy ECO_0000203 NP558791.RAQrx-eIgApE1XHzQV6JXiLDdTEgZiZn0nVtUJxCPm6GY130_provenance.
- NP558791.RAQrx-eIgApE1XHzQV6JXiLDdTEgZiZn0nVtUJxCPm6GY130_assertion wasDerivedFrom befree-20140225 NP558791.RAQrx-eIgApE1XHzQV6JXiLDdTEgZiZn0nVtUJxCPm6GY130_provenance.
- NP558791.RAQrx-eIgApE1XHzQV6JXiLDdTEgZiZn0nVtUJxCPm6GY130_assertion SIO_000772 11393670 NP558791.RAQrx-eIgApE1XHzQV6JXiLDdTEgZiZn0nVtUJxCPm6GY130_provenance.
- NP558791.RAQrx-eIgApE1XHzQV6JXiLDdTEgZiZn0nVtUJxCPm6GY130_assertion evidence source_evidence_literature NP558791.RAQrx-eIgApE1XHzQV6JXiLDdTEgZiZn0nVtUJxCPm6GY130_provenance.
- NP558791.RAQrx-eIgApE1XHzQV6JXiLDdTEgZiZn0nVtUJxCPm6GY130_assertion description "[AGT M235T and ATR A1166C allele and genotype frequencies were similar between CAD and CAD-free patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP558791.RAQrx-eIgApE1XHzQV6JXiLDdTEgZiZn0nVtUJxCPm6GY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP558791.RAQrx-eIgApE1XHzQV6JXiLDdTEgZiZn0nVtUJxCPm6GY130_provenance.