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- source_evidence_literature type ECO_0000212 NP1372698.RAgifQPGnM4F6hhjqCe0J-8xyzp0nC62LfJspxCGn42F8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1372698.RAgifQPGnM4F6hhjqCe0J-8xyzp0nC62LfJspxCGn42F8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1372698.RAgifQPGnM4F6hhjqCe0J-8xyzp0nC62LfJspxCGn42F8130_provenance.
- NP1372698.RAgifQPGnM4F6hhjqCe0J-8xyzp0nC62LfJspxCGn42F8130_assertion description "[We have reported frequent allele loss for the marker HRAS on chromosome 11p in human lung cancer and defined the smallest common region of deletion (designated LOH11B) to approximately 500 kb.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1372698.RAgifQPGnM4F6hhjqCe0J-8xyzp0nC62LfJspxCGn42F8130_provenance.
- NP1372698.RAgifQPGnM4F6hhjqCe0J-8xyzp0nC62LfJspxCGn42F8130_assertion evidence source_evidence_literature NP1372698.RAgifQPGnM4F6hhjqCe0J-8xyzp0nC62LfJspxCGn42F8130_provenance.
- NP1372698.RAgifQPGnM4F6hhjqCe0J-8xyzp0nC62LfJspxCGn42F8130_assertion SIO_000772 9149890 NP1372698.RAgifQPGnM4F6hhjqCe0J-8xyzp0nC62LfJspxCGn42F8130_provenance.
- NP1372698.RAgifQPGnM4F6hhjqCe0J-8xyzp0nC62LfJspxCGn42F8130_assertion wasDerivedFrom befree-2016 NP1372698.RAgifQPGnM4F6hhjqCe0J-8xyzp0nC62LfJspxCGn42F8130_provenance.
- NP1372698.RAgifQPGnM4F6hhjqCe0J-8xyzp0nC62LfJspxCGn42F8130_assertion wasGeneratedBy ECO_0000203 NP1372698.RAgifQPGnM4F6hhjqCe0J-8xyzp0nC62LfJspxCGn42F8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1372698.RAgifQPGnM4F6hhjqCe0J-8xyzp0nC62LfJspxCGn42F8130_provenance.