Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP800280.RAQEeJo3dpFOwe7V2pKKeBRfYA7_p-YamKmBBrwovWM8E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP800280.RAQEeJo3dpFOwe7V2pKKeBRfYA7_p-YamKmBBrwovWM8E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800280.RAQEeJo3dpFOwe7V2pKKeBRfYA7_p-YamKmBBrwovWM8E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800280.RAQEeJo3dpFOwe7V2pKKeBRfYA7_p-YamKmBBrwovWM8E130_provenance.
- NP800280.RAQEeJo3dpFOwe7V2pKKeBRfYA7_p-YamKmBBrwovWM8E130_assertion description "[The G13964C intronic variant was significantly associated with familial breast cancer risk (p=0.0018) while the genotypic distribution was similar for p53 Arg72Pro and Ins16bp in patients and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800280.RAQEeJo3dpFOwe7V2pKKeBRfYA7_p-YamKmBBrwovWM8E130_provenance.
- NP800280.RAQEeJo3dpFOwe7V2pKKeBRfYA7_p-YamKmBBrwovWM8E130_assertion evidence source_evidence_literature NP800280.RAQEeJo3dpFOwe7V2pKKeBRfYA7_p-YamKmBBrwovWM8E130_provenance.
- NP800280.RAQEeJo3dpFOwe7V2pKKeBRfYA7_p-YamKmBBrwovWM8E130_assertion SIO_000772 20233677 NP800280.RAQEeJo3dpFOwe7V2pKKeBRfYA7_p-YamKmBBrwovWM8E130_provenance.
- NP800280.RAQEeJo3dpFOwe7V2pKKeBRfYA7_p-YamKmBBrwovWM8E130_assertion wasDerivedFrom befree-2016 NP800280.RAQEeJo3dpFOwe7V2pKKeBRfYA7_p-YamKmBBrwovWM8E130_provenance.
- NP800280.RAQEeJo3dpFOwe7V2pKKeBRfYA7_p-YamKmBBrwovWM8E130_assertion wasGeneratedBy ECO_0000203 NP800280.RAQEeJo3dpFOwe7V2pKKeBRfYA7_p-YamKmBBrwovWM8E130_provenance.
- befree-2016 importedOn "2016-02-19" NP800280.RAQEeJo3dpFOwe7V2pKKeBRfYA7_p-YamKmBBrwovWM8E130_provenance.