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- source_evidence_literature type ECO_0000212 NP116824.RAeF2XN2NxfyNWDBdZDu1SRcCH7mBMBaz7RAnL1k5NkIM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP116824.RAeF2XN2NxfyNWDBdZDu1SRcCH7mBMBaz7RAnL1k5NkIM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP116824.RAeF2XN2NxfyNWDBdZDu1SRcCH7mBMBaz7RAnL1k5NkIM130_provenance.
- NP116824.RAeF2XN2NxfyNWDBdZDu1SRcCH7mBMBaz7RAnL1k5NkIM130_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." NP116824.RAeF2XN2NxfyNWDBdZDu1SRcCH7mBMBaz7RAnL1k5NkIM130_provenance.
- NP116824.RAeF2XN2NxfyNWDBdZDu1SRcCH7mBMBaz7RAnL1k5NkIM130_assertion evidence source_evidence_literature NP116824.RAeF2XN2NxfyNWDBdZDu1SRcCH7mBMBaz7RAnL1k5NkIM130_provenance.
- NP116824.RAeF2XN2NxfyNWDBdZDu1SRcCH7mBMBaz7RAnL1k5NkIM130_assertion SIO_000772 19008095 NP116824.RAeF2XN2NxfyNWDBdZDu1SRcCH7mBMBaz7RAnL1k5NkIM130_provenance.
- NP116824.RAeF2XN2NxfyNWDBdZDu1SRcCH7mBMBaz7RAnL1k5NkIM130_assertion wasDerivedFrom gad-20150221 NP116824.RAeF2XN2NxfyNWDBdZDu1SRcCH7mBMBaz7RAnL1k5NkIM130_provenance.
- NP116824.RAeF2XN2NxfyNWDBdZDu1SRcCH7mBMBaz7RAnL1k5NkIM130_assertion wasGeneratedBy ECO_0000203 NP116824.RAeF2XN2NxfyNWDBdZDu1SRcCH7mBMBaz7RAnL1k5NkIM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP116824.RAeF2XN2NxfyNWDBdZDu1SRcCH7mBMBaz7RAnL1k5NkIM130_provenance.