Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP214021.RALG9jxlreMdR3TkKcc014lENqgU1dFOLygrfAPva96_Y130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP214021.RALG9jxlreMdR3TkKcc014lENqgU1dFOLygrfAPva96_Y130_assertion type Assertion NP214021.RALG9jxlreMdR3TkKcc014lENqgU1dFOLygrfAPva96_Y130_head.
- 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.