Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP66392.RAVE-LG9FH4ASXD5N0EP_8eYbSJaHN0Qo71U-GevP3EeI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP66392.RAVE-LG9FH4ASXD5N0EP_8eYbSJaHN0Qo71U-GevP3EeI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP66392.RAVE-LG9FH4ASXD5N0EP_8eYbSJaHN0Qo71U-GevP3EeI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP66392.RAVE-LG9FH4ASXD5N0EP_8eYbSJaHN0Qo71U-GevP3EeI130_provenance.
- NP66392.RAVE-LG9FH4ASXD5N0EP_8eYbSJaHN0Qo71U-GevP3EeI130_assertion description "[We investigated whether putatively functional single nucleotide polymorphisms (SNPs) in genes related to CIN (CENPF, ESPL1, NEK2, PTTG1, ZWILCH, ZWINT) affect breast cancer (BC) risk and clinical outcome in a Swedish cohort of 749 incident BC cases with detailed clinical data and up to 15 years of follow-up and 1493 matched controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66392.RAVE-LG9FH4ASXD5N0EP_8eYbSJaHN0Qo71U-GevP3EeI130_provenance.
- NP66392.RAVE-LG9FH4ASXD5N0EP_8eYbSJaHN0Qo71U-GevP3EeI130_assertion evidence source_evidence_literature NP66392.RAVE-LG9FH4ASXD5N0EP_8eYbSJaHN0Qo71U-GevP3EeI130_provenance.
- NP66392.RAVE-LG9FH4ASXD5N0EP_8eYbSJaHN0Qo71U-GevP3EeI130_assertion SIO_000772 19008095 NP66392.RAVE-LG9FH4ASXD5N0EP_8eYbSJaHN0Qo71U-GevP3EeI130_provenance.
- NP66392.RAVE-LG9FH4ASXD5N0EP_8eYbSJaHN0Qo71U-GevP3EeI130_assertion wasDerivedFrom gad-20130706 NP66392.RAVE-LG9FH4ASXD5N0EP_8eYbSJaHN0Qo71U-GevP3EeI130_provenance.
- NP66392.RAVE-LG9FH4ASXD5N0EP_8eYbSJaHN0Qo71U-GevP3EeI130_assertion wasGeneratedBy ECO_0000203 NP66392.RAVE-LG9FH4ASXD5N0EP_8eYbSJaHN0Qo71U-GevP3EeI130_provenance.
- gad-20130706 importedOn "2013-07-06" NP66392.RAVE-LG9FH4ASXD5N0EP_8eYbSJaHN0Qo71U-GevP3EeI130_provenance.