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- source_evidence_literature type ECO_0000212 NP1244690.RAZpwnpeotp7aG_m-jogwom-Jep0SxKcwpxCsayc_59Oc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1244690.RAZpwnpeotp7aG_m-jogwom-Jep0SxKcwpxCsayc_59Oc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1244690.RAZpwnpeotp7aG_m-jogwom-Jep0SxKcwpxCsayc_59Oc130_provenance.
- NP1244690.RAZpwnpeotp7aG_m-jogwom-Jep0SxKcwpxCsayc_59Oc130_assertion description "[ECCCs had SCA-like features with rare expression of estrogen receptor/progesterone receptor (18.8%/6.3%) and no K-RAS mutations, intermediate features regarding expressions of p53 (37.5%) and p16 (25%), and endometrioid adenocarcinoma-like features regarding losses of PTEN (81.3%), ARID1A (25%) and mismatch-repair protein (68.8%), expression of microsatellite instability-high (25%), HER2/neu (12.5%), and PIK3CA mutations (18.8%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244690.RAZpwnpeotp7aG_m-jogwom-Jep0SxKcwpxCsayc_59Oc130_provenance.
- NP1244690.RAZpwnpeotp7aG_m-jogwom-Jep0SxKcwpxCsayc_59Oc130_assertion evidence source_evidence_literature NP1244690.RAZpwnpeotp7aG_m-jogwom-Jep0SxKcwpxCsayc_59Oc130_provenance.
- NP1244690.RAZpwnpeotp7aG_m-jogwom-Jep0SxKcwpxCsayc_59Oc130_assertion SIO_000772 25473756 NP1244690.RAZpwnpeotp7aG_m-jogwom-Jep0SxKcwpxCsayc_59Oc130_provenance.
- NP1244690.RAZpwnpeotp7aG_m-jogwom-Jep0SxKcwpxCsayc_59Oc130_assertion wasDerivedFrom befree-2016 NP1244690.RAZpwnpeotp7aG_m-jogwom-Jep0SxKcwpxCsayc_59Oc130_provenance.
- NP1244690.RAZpwnpeotp7aG_m-jogwom-Jep0SxKcwpxCsayc_59Oc130_assertion wasGeneratedBy ECO_0000203 NP1244690.RAZpwnpeotp7aG_m-jogwom-Jep0SxKcwpxCsayc_59Oc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1244690.RAZpwnpeotp7aG_m-jogwom-Jep0SxKcwpxCsayc_59Oc130_provenance.