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- source_evidence_literature type ECO_0000212 NP183001.RAaBd-1YKdWXE7CTBDwJHlEv6zr5aH9I-iOzQ58enHDZw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP183001.RAaBd-1YKdWXE7CTBDwJHlEv6zr5aH9I-iOzQ58enHDZw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP183001.RAaBd-1YKdWXE7CTBDwJHlEv6zr5aH9I-iOzQ58enHDZw130_provenance.
- NP183001.RAaBd-1YKdWXE7CTBDwJHlEv6zr5aH9I-iOzQ58enHDZw130_assertion description "[Overall promoter methylation (OPM) in the SFRP2 gene was observed in one N and four T, whereas partial promoter methylation (PPM) was observed in two N and five T. OPM in the P16 gene was present in one T. In the DAPK1 gene, OPM existed in seven T and five N, while PPM was present in two N. In the HIC1 gene, OPM was demonstrated in three T, while PPM was noted in two N; however, no methylation existed in N. In the MGMT gene, OPM occurred in five T and two N, and PPM was present in one T. KRAS mutations in Turkish patients with SCRC are similar to those of other population groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183001.RAaBd-1YKdWXE7CTBDwJHlEv6zr5aH9I-iOzQ58enHDZw130_provenance.
- NP183001.RAaBd-1YKdWXE7CTBDwJHlEv6zr5aH9I-iOzQ58enHDZw130_assertion evidence source_evidence_literature NP183001.RAaBd-1YKdWXE7CTBDwJHlEv6zr5aH9I-iOzQ58enHDZw130_provenance.
- NP183001.RAaBd-1YKdWXE7CTBDwJHlEv6zr5aH9I-iOzQ58enHDZw130_assertion SIO_000772 20682398 NP183001.RAaBd-1YKdWXE7CTBDwJHlEv6zr5aH9I-iOzQ58enHDZw130_provenance.
- NP183001.RAaBd-1YKdWXE7CTBDwJHlEv6zr5aH9I-iOzQ58enHDZw130_assertion wasDerivedFrom gad-20150221 NP183001.RAaBd-1YKdWXE7CTBDwJHlEv6zr5aH9I-iOzQ58enHDZw130_provenance.
- NP183001.RAaBd-1YKdWXE7CTBDwJHlEv6zr5aH9I-iOzQ58enHDZw130_assertion wasGeneratedBy ECO_0000203 NP183001.RAaBd-1YKdWXE7CTBDwJHlEv6zr5aH9I-iOzQ58enHDZw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP183001.RAaBd-1YKdWXE7CTBDwJHlEv6zr5aH9I-iOzQ58enHDZw130_provenance.