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- source_evidence_literature type ECO_0000212 NP904427.RAd7x2gf2QwMvkCzF60rpj9mGjDapBUBSFP_JPmucuuYU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP904427.RAd7x2gf2QwMvkCzF60rpj9mGjDapBUBSFP_JPmucuuYU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP904427.RAd7x2gf2QwMvkCzF60rpj9mGjDapBUBSFP_JPmucuuYU130_provenance.
- NP904427.RAd7x2gf2QwMvkCzF60rpj9mGjDapBUBSFP_JPmucuuYU130_assertion description "[We identify three new CIN-suppressor genes (PIGN (also known as MCD4), MEX3C (RKHD2) and ZNF516 (KIAA0222)) encoded on chromosome 18q that are subject to frequent copy number loss in CIN(+) CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP904427.RAd7x2gf2QwMvkCzF60rpj9mGjDapBUBSFP_JPmucuuYU130_provenance.
- NP904427.RAd7x2gf2QwMvkCzF60rpj9mGjDapBUBSFP_JPmucuuYU130_assertion evidence source_evidence_literature NP904427.RAd7x2gf2QwMvkCzF60rpj9mGjDapBUBSFP_JPmucuuYU130_provenance.
- NP904427.RAd7x2gf2QwMvkCzF60rpj9mGjDapBUBSFP_JPmucuuYU130_assertion SIO_000772 23446422 NP904427.RAd7x2gf2QwMvkCzF60rpj9mGjDapBUBSFP_JPmucuuYU130_provenance.
- NP904427.RAd7x2gf2QwMvkCzF60rpj9mGjDapBUBSFP_JPmucuuYU130_assertion wasDerivedFrom befree-20150227 NP904427.RAd7x2gf2QwMvkCzF60rpj9mGjDapBUBSFP_JPmucuuYU130_provenance.
- NP904427.RAd7x2gf2QwMvkCzF60rpj9mGjDapBUBSFP_JPmucuuYU130_assertion wasGeneratedBy ECO_0000203 NP904427.RAd7x2gf2QwMvkCzF60rpj9mGjDapBUBSFP_JPmucuuYU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP904427.RAd7x2gf2QwMvkCzF60rpj9mGjDapBUBSFP_JPmucuuYU130_provenance.