Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP580256.RAXDktNJygREHO15lYHd-0gc3FmJzPwlo_-PGejV9_jXI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP580256.RAXDktNJygREHO15lYHd-0gc3FmJzPwlo_-PGejV9_jXI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP580256.RAXDktNJygREHO15lYHd-0gc3FmJzPwlo_-PGejV9_jXI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP580256.RAXDktNJygREHO15lYHd-0gc3FmJzPwlo_-PGejV9_jXI130_provenance.
- NP580256.RAXDktNJygREHO15lYHd-0gc3FmJzPwlo_-PGejV9_jXI130_assertion description "[We used a genetic association study design to determine if common genetic variation (frequency>or=5%) in a 400-kb region surrounding ERBB2 and containing the PPARBP, CRK7, NEUROD2, PPP1R1B, STARD3, TCAP, PNMT, CAB2, ERBB2, C17ORF37, GRB7 and ZNFN1A3 genes, was associated with breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP580256.RAXDktNJygREHO15lYHd-0gc3FmJzPwlo_-PGejV9_jXI130_provenance.
- NP580256.RAXDktNJygREHO15lYHd-0gc3FmJzPwlo_-PGejV9_jXI130_assertion evidence source_evidence_literature NP580256.RAXDktNJygREHO15lYHd-0gc3FmJzPwlo_-PGejV9_jXI130_provenance.
- NP580256.RAXDktNJygREHO15lYHd-0gc3FmJzPwlo_-PGejV9_jXI130_assertion SIO_000772 17117180 NP580256.RAXDktNJygREHO15lYHd-0gc3FmJzPwlo_-PGejV9_jXI130_provenance.
- NP580256.RAXDktNJygREHO15lYHd-0gc3FmJzPwlo_-PGejV9_jXI130_assertion wasDerivedFrom befree-2016 NP580256.RAXDktNJygREHO15lYHd-0gc3FmJzPwlo_-PGejV9_jXI130_provenance.
- NP580256.RAXDktNJygREHO15lYHd-0gc3FmJzPwlo_-PGejV9_jXI130_assertion wasGeneratedBy ECO_0000203 NP580256.RAXDktNJygREHO15lYHd-0gc3FmJzPwlo_-PGejV9_jXI130_provenance.
- befree-2016 importedOn "2016-02-19" NP580256.RAXDktNJygREHO15lYHd-0gc3FmJzPwlo_-PGejV9_jXI130_provenance.