Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP906735.RAAJZLfyW6oS8m1VPjXxeFkj4bwLjm53mmnm1ubu_dc3k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP906735.RAAJZLfyW6oS8m1VPjXxeFkj4bwLjm53mmnm1ubu_dc3k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP906735.RAAJZLfyW6oS8m1VPjXxeFkj4bwLjm53mmnm1ubu_dc3k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP906735.RAAJZLfyW6oS8m1VPjXxeFkj4bwLjm53mmnm1ubu_dc3k130_provenance.
- NP906735.RAAJZLfyW6oS8m1VPjXxeFkj4bwLjm53mmnm1ubu_dc3k130_assertion description "[CCND2 is often overexpressed in chronic B-cell disorders, and we recently detected genomic amplification of the chromosomal region containing CCND2 in two of three investigated non-Hodgkin lymphomas (NHLs) with cytogenetic abnormalities involving 12p.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP906735.RAAJZLfyW6oS8m1VPjXxeFkj4bwLjm53mmnm1ubu_dc3k130_provenance.
- NP906735.RAAJZLfyW6oS8m1VPjXxeFkj4bwLjm53mmnm1ubu_dc3k130_assertion evidence source_evidence_literature NP906735.RAAJZLfyW6oS8m1VPjXxeFkj4bwLjm53mmnm1ubu_dc3k130_provenance.
- NP906735.RAAJZLfyW6oS8m1VPjXxeFkj4bwLjm53mmnm1ubu_dc3k130_assertion SIO_000772 9530346 NP906735.RAAJZLfyW6oS8m1VPjXxeFkj4bwLjm53mmnm1ubu_dc3k130_provenance.
- NP906735.RAAJZLfyW6oS8m1VPjXxeFkj4bwLjm53mmnm1ubu_dc3k130_assertion wasDerivedFrom befree-20140225 NP906735.RAAJZLfyW6oS8m1VPjXxeFkj4bwLjm53mmnm1ubu_dc3k130_provenance.
- NP906735.RAAJZLfyW6oS8m1VPjXxeFkj4bwLjm53mmnm1ubu_dc3k130_assertion wasGeneratedBy ECO_0000203 NP906735.RAAJZLfyW6oS8m1VPjXxeFkj4bwLjm53mmnm1ubu_dc3k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP906735.RAAJZLfyW6oS8m1VPjXxeFkj4bwLjm53mmnm1ubu_dc3k130_provenance.