Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP904605.RAbPCiSrQWVRw22zqpv3R_QS0IQ8ztDTcFoPRUaIS-NjQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP904605.RAbPCiSrQWVRw22zqpv3R_QS0IQ8ztDTcFoPRUaIS-NjQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP904605.RAbPCiSrQWVRw22zqpv3R_QS0IQ8ztDTcFoPRUaIS-NjQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP904605.RAbPCiSrQWVRw22zqpv3R_QS0IQ8ztDTcFoPRUaIS-NjQ130_provenance.
- NP904605.RAbPCiSrQWVRw22zqpv3R_QS0IQ8ztDTcFoPRUaIS-NjQ130_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." NP904605.RAbPCiSrQWVRw22zqpv3R_QS0IQ8ztDTcFoPRUaIS-NjQ130_provenance.
- NP904605.RAbPCiSrQWVRw22zqpv3R_QS0IQ8ztDTcFoPRUaIS-NjQ130_assertion evidence source_evidence_literature NP904605.RAbPCiSrQWVRw22zqpv3R_QS0IQ8ztDTcFoPRUaIS-NjQ130_provenance.
- NP904605.RAbPCiSrQWVRw22zqpv3R_QS0IQ8ztDTcFoPRUaIS-NjQ130_assertion SIO_000772 14997935 NP904605.RAbPCiSrQWVRw22zqpv3R_QS0IQ8ztDTcFoPRUaIS-NjQ130_provenance.
- NP904605.RAbPCiSrQWVRw22zqpv3R_QS0IQ8ztDTcFoPRUaIS-NjQ130_assertion wasDerivedFrom befree-20140225 NP904605.RAbPCiSrQWVRw22zqpv3R_QS0IQ8ztDTcFoPRUaIS-NjQ130_provenance.
- NP904605.RAbPCiSrQWVRw22zqpv3R_QS0IQ8ztDTcFoPRUaIS-NjQ130_assertion wasGeneratedBy ECO_0000203 NP904605.RAbPCiSrQWVRw22zqpv3R_QS0IQ8ztDTcFoPRUaIS-NjQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP904605.RAbPCiSrQWVRw22zqpv3R_QS0IQ8ztDTcFoPRUaIS-NjQ130_provenance.