Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP214021.RALG9jxlreMdR3TkKcc014lENqgU1dFOLygrfAPva96_Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP214021.RALG9jxlreMdR3TkKcc014lENqgU1dFOLygrfAPva96_Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP214021.RALG9jxlreMdR3TkKcc014lENqgU1dFOLygrfAPva96_Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP214021.RALG9jxlreMdR3TkKcc014lENqgU1dFOLygrfAPva96_Y130_provenance.
- NP214021.RALG9jxlreMdR3TkKcc014lENqgU1dFOLygrfAPva96_Y130_assertion description "[Association of a null allele of SPRN with variant Creutzfeldt-Jakob disease]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP214021.RALG9jxlreMdR3TkKcc014lENqgU1dFOLygrfAPva96_Y130_provenance.
- NP214021.RALG9jxlreMdR3TkKcc014lENqgU1dFOLygrfAPva96_Y130_assertion evidence source_evidence_literature NP214021.RALG9jxlreMdR3TkKcc014lENqgU1dFOLygrfAPva96_Y130_provenance.
- NP214021.RALG9jxlreMdR3TkKcc014lENqgU1dFOLygrfAPva96_Y130_assertion SIO_000772 18805828 NP214021.RALG9jxlreMdR3TkKcc014lENqgU1dFOLygrfAPva96_Y130_provenance.
- NP214021.RALG9jxlreMdR3TkKcc014lENqgU1dFOLygrfAPva96_Y130_assertion wasDerivedFrom lhgdn-20090331 NP214021.RALG9jxlreMdR3TkKcc014lENqgU1dFOLygrfAPva96_Y130_provenance.
- NP214021.RALG9jxlreMdR3TkKcc014lENqgU1dFOLygrfAPva96_Y130_assertion wasGeneratedBy ECO_0000203 NP214021.RALG9jxlreMdR3TkKcc014lENqgU1dFOLygrfAPva96_Y130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP214021.RALG9jxlreMdR3TkKcc014lENqgU1dFOLygrfAPva96_Y130_provenance.