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- source_evidence_literature type ECO_0000212 NP274906.RALECTw98U7h8X5QLN_Y1f3OUN62M2r2SwjM076ZB9i4c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP274906.RALECTw98U7h8X5QLN_Y1f3OUN62M2r2SwjM076ZB9i4c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP274906.RALECTw98U7h8X5QLN_Y1f3OUN62M2r2SwjM076ZB9i4c130_provenance.
- NP274906.RALECTw98U7h8X5QLN_Y1f3OUN62M2r2SwjM076ZB9i4c130_assertion description "[The mutation causing myotonic dystrophy (DM) has recently been identified as an unstable CTG trinucleotide repeat located in the 3' untranslated region of a gene encoding for a protein with putative serine-threonine protein kinase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274906.RALECTw98U7h8X5QLN_Y1f3OUN62M2r2SwjM076ZB9i4c130_provenance.
- NP274906.RALECTw98U7h8X5QLN_Y1f3OUN62M2r2SwjM076ZB9i4c130_assertion evidence source_evidence_literature NP274906.RALECTw98U7h8X5QLN_Y1f3OUN62M2r2SwjM076ZB9i4c130_provenance.
- NP274906.RALECTw98U7h8X5QLN_Y1f3OUN62M2r2SwjM076ZB9i4c130_assertion SIO_000772 8499920 NP274906.RALECTw98U7h8X5QLN_Y1f3OUN62M2r2SwjM076ZB9i4c130_provenance.
- NP274906.RALECTw98U7h8X5QLN_Y1f3OUN62M2r2SwjM076ZB9i4c130_assertion wasDerivedFrom befree-20150227 NP274906.RALECTw98U7h8X5QLN_Y1f3OUN62M2r2SwjM076ZB9i4c130_provenance.
- NP274906.RALECTw98U7h8X5QLN_Y1f3OUN62M2r2SwjM076ZB9i4c130_assertion wasGeneratedBy ECO_0000203 NP274906.RALECTw98U7h8X5QLN_Y1f3OUN62M2r2SwjM076ZB9i4c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP274906.RALECTw98U7h8X5QLN_Y1f3OUN62M2r2SwjM076ZB9i4c130_provenance.