Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP399207.RAOTmU0lVkdoHsnEUxYPdiIA9L4_NTiekQAhHar_NDt10130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP399207.RAOTmU0lVkdoHsnEUxYPdiIA9L4_NTiekQAhHar_NDt10130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP399207.RAOTmU0lVkdoHsnEUxYPdiIA9L4_NTiekQAhHar_NDt10130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP399207.RAOTmU0lVkdoHsnEUxYPdiIA9L4_NTiekQAhHar_NDt10130_provenance.
- NP399207.RAOTmU0lVkdoHsnEUxYPdiIA9L4_NTiekQAhHar_NDt10130_assertion description "[SNUOT-RB1 and SNUOT-RB4 gained chromosomal copy numbers commonly in chromosome 11, especially in locus 11q13, which is responsible for cancer-related genes such as CCND1, MEN1, and FGF3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP399207.RAOTmU0lVkdoHsnEUxYPdiIA9L4_NTiekQAhHar_NDt10130_provenance.
- NP399207.RAOTmU0lVkdoHsnEUxYPdiIA9L4_NTiekQAhHar_NDt10130_assertion evidence source_evidence_literature NP399207.RAOTmU0lVkdoHsnEUxYPdiIA9L4_NTiekQAhHar_NDt10130_provenance.
- NP399207.RAOTmU0lVkdoHsnEUxYPdiIA9L4_NTiekQAhHar_NDt10130_assertion SIO_000772 18799932 NP399207.RAOTmU0lVkdoHsnEUxYPdiIA9L4_NTiekQAhHar_NDt10130_provenance.
- NP399207.RAOTmU0lVkdoHsnEUxYPdiIA9L4_NTiekQAhHar_NDt10130_assertion wasDerivedFrom befree-20150227 NP399207.RAOTmU0lVkdoHsnEUxYPdiIA9L4_NTiekQAhHar_NDt10130_provenance.
- NP399207.RAOTmU0lVkdoHsnEUxYPdiIA9L4_NTiekQAhHar_NDt10130_assertion wasGeneratedBy ECO_0000203 NP399207.RAOTmU0lVkdoHsnEUxYPdiIA9L4_NTiekQAhHar_NDt10130_provenance.
- befree-20150227 importedOn "2015-02-27" NP399207.RAOTmU0lVkdoHsnEUxYPdiIA9L4_NTiekQAhHar_NDt10130_provenance.