Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP562524.RAVndpntQpBnFwC5dXN0w1QC_BPVpRXWPpnMHiLr3vT40130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP562524.RAVndpntQpBnFwC5dXN0w1QC_BPVpRXWPpnMHiLr3vT40130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP562524.RAVndpntQpBnFwC5dXN0w1QC_BPVpRXWPpnMHiLr3vT40130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP562524.RAVndpntQpBnFwC5dXN0w1QC_BPVpRXWPpnMHiLr3vT40130_provenance.
- NP562524.RAVndpntQpBnFwC5dXN0w1QC_BPVpRXWPpnMHiLr3vT40130_assertion description "[Selenoprotein N (SelN) is the only selenoprotein involved in a genetic disease; its function being unknown, no treatment is available for this potentially lethal disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP562524.RAVndpntQpBnFwC5dXN0w1QC_BPVpRXWPpnMHiLr3vT40130_provenance.
- NP562524.RAVndpntQpBnFwC5dXN0w1QC_BPVpRXWPpnMHiLr3vT40130_assertion evidence source_evidence_literature NP562524.RAVndpntQpBnFwC5dXN0w1QC_BPVpRXWPpnMHiLr3vT40130_provenance.
- NP562524.RAVndpntQpBnFwC5dXN0w1QC_BPVpRXWPpnMHiLr3vT40130_assertion SIO_000772 19557870 NP562524.RAVndpntQpBnFwC5dXN0w1QC_BPVpRXWPpnMHiLr3vT40130_provenance.
- NP562524.RAVndpntQpBnFwC5dXN0w1QC_BPVpRXWPpnMHiLr3vT40130_assertion wasDerivedFrom befree-20140225 NP562524.RAVndpntQpBnFwC5dXN0w1QC_BPVpRXWPpnMHiLr3vT40130_provenance.
- NP562524.RAVndpntQpBnFwC5dXN0w1QC_BPVpRXWPpnMHiLr3vT40130_assertion wasGeneratedBy ECO_0000203 NP562524.RAVndpntQpBnFwC5dXN0w1QC_BPVpRXWPpnMHiLr3vT40130_provenance.
- befree-20140225 importedOn "2014-02-25" NP562524.RAVndpntQpBnFwC5dXN0w1QC_BPVpRXWPpnMHiLr3vT40130_provenance.