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- source_evidence_literature type ECO_0000212 NP1114911.RA08-xQ1NG_6evw8A-3IOWFB3bNPavaq_ohSPsscO5A_Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1114911.RA08-xQ1NG_6evw8A-3IOWFB3bNPavaq_ohSPsscO5A_Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1114911.RA08-xQ1NG_6evw8A-3IOWFB3bNPavaq_ohSPsscO5A_Y130_provenance.
- NP1114911.RA08-xQ1NG_6evw8A-3IOWFB3bNPavaq_ohSPsscO5A_Y130_assertion description "[However, the progressive and severe cerebellar atrophy seen in the affected individuals could indicate an evolutionarily unique role for GRID2 in the human cerebellum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1114911.RA08-xQ1NG_6evw8A-3IOWFB3bNPavaq_ohSPsscO5A_Y130_provenance.
- NP1114911.RA08-xQ1NG_6evw8A-3IOWFB3bNPavaq_ohSPsscO5A_Y130_assertion evidence source_evidence_literature NP1114911.RA08-xQ1NG_6evw8A-3IOWFB3bNPavaq_ohSPsscO5A_Y130_provenance.
- NP1114911.RA08-xQ1NG_6evw8A-3IOWFB3bNPavaq_ohSPsscO5A_Y130_assertion SIO_000772 24078737 NP1114911.RA08-xQ1NG_6evw8A-3IOWFB3bNPavaq_ohSPsscO5A_Y130_provenance.
- NP1114911.RA08-xQ1NG_6evw8A-3IOWFB3bNPavaq_ohSPsscO5A_Y130_assertion wasDerivedFrom befree-2016 NP1114911.RA08-xQ1NG_6evw8A-3IOWFB3bNPavaq_ohSPsscO5A_Y130_provenance.
- NP1114911.RA08-xQ1NG_6evw8A-3IOWFB3bNPavaq_ohSPsscO5A_Y130_assertion wasGeneratedBy ECO_0000203 NP1114911.RA08-xQ1NG_6evw8A-3IOWFB3bNPavaq_ohSPsscO5A_Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP1114911.RA08-xQ1NG_6evw8A-3IOWFB3bNPavaq_ohSPsscO5A_Y130_provenance.