Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP433988.RA20idRzlH6rN6NCzD63zaTQFCWOE875HvOV_xoGRZ-6Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP433988.RA20idRzlH6rN6NCzD63zaTQFCWOE875HvOV_xoGRZ-6Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP433988.RA20idRzlH6rN6NCzD63zaTQFCWOE875HvOV_xoGRZ-6Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP433988.RA20idRzlH6rN6NCzD63zaTQFCWOE875HvOV_xoGRZ-6Q130_provenance.
- NP433988.RA20idRzlH6rN6NCzD63zaTQFCWOE875HvOV_xoGRZ-6Q130_assertion description "[Remarkably, most of the genes showing distinctive expression in oligodendroglioma with 1p loss were also highly expressed in normal brain tissues and had neuron-related function, which included MYT1L, INA, RIMS2, SNAP97 and SNCB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP433988.RA20idRzlH6rN6NCzD63zaTQFCWOE875HvOV_xoGRZ-6Q130_provenance.
- NP433988.RA20idRzlH6rN6NCzD63zaTQFCWOE875HvOV_xoGRZ-6Q130_assertion evidence source_evidence_literature NP433988.RA20idRzlH6rN6NCzD63zaTQFCWOE875HvOV_xoGRZ-6Q130_provenance.
- NP433988.RA20idRzlH6rN6NCzD63zaTQFCWOE875HvOV_xoGRZ-6Q130_assertion SIO_000772 14997935 NP433988.RA20idRzlH6rN6NCzD63zaTQFCWOE875HvOV_xoGRZ-6Q130_provenance.
- NP433988.RA20idRzlH6rN6NCzD63zaTQFCWOE875HvOV_xoGRZ-6Q130_assertion wasDerivedFrom befree-2016 NP433988.RA20idRzlH6rN6NCzD63zaTQFCWOE875HvOV_xoGRZ-6Q130_provenance.
- NP433988.RA20idRzlH6rN6NCzD63zaTQFCWOE875HvOV_xoGRZ-6Q130_assertion wasGeneratedBy ECO_0000203 NP433988.RA20idRzlH6rN6NCzD63zaTQFCWOE875HvOV_xoGRZ-6Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP433988.RA20idRzlH6rN6NCzD63zaTQFCWOE875HvOV_xoGRZ-6Q130_provenance.