Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP480360.RAP88-naLpWtb5SWZW_CtZ8nk_e6ryTH56xxu9Fww-Mv8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP480360.RAP88-naLpWtb5SWZW_CtZ8nk_e6ryTH56xxu9Fww-Mv8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP480360.RAP88-naLpWtb5SWZW_CtZ8nk_e6ryTH56xxu9Fww-Mv8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP480360.RAP88-naLpWtb5SWZW_CtZ8nk_e6ryTH56xxu9Fww-Mv8130_provenance.
- NP480360.RAP88-naLpWtb5SWZW_CtZ8nk_e6ryTH56xxu9Fww-Mv8130_assertion description "[Genetic studies excluded mutations in the DM type 1 (DM1) gene, but revealed a CCTG repeat expansion in the ZNF9 gene, which is associated with DM2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480360.RAP88-naLpWtb5SWZW_CtZ8nk_e6ryTH56xxu9Fww-Mv8130_provenance.
- NP480360.RAP88-naLpWtb5SWZW_CtZ8nk_e6ryTH56xxu9Fww-Mv8130_assertion evidence source_evidence_literature NP480360.RAP88-naLpWtb5SWZW_CtZ8nk_e6ryTH56xxu9Fww-Mv8130_provenance.
- NP480360.RAP88-naLpWtb5SWZW_CtZ8nk_e6ryTH56xxu9Fww-Mv8130_assertion SIO_000772 15704146 NP480360.RAP88-naLpWtb5SWZW_CtZ8nk_e6ryTH56xxu9Fww-Mv8130_provenance.
- NP480360.RAP88-naLpWtb5SWZW_CtZ8nk_e6ryTH56xxu9Fww-Mv8130_assertion wasDerivedFrom befree-2016 NP480360.RAP88-naLpWtb5SWZW_CtZ8nk_e6ryTH56xxu9Fww-Mv8130_provenance.
- NP480360.RAP88-naLpWtb5SWZW_CtZ8nk_e6ryTH56xxu9Fww-Mv8130_assertion wasGeneratedBy ECO_0000203 NP480360.RAP88-naLpWtb5SWZW_CtZ8nk_e6ryTH56xxu9Fww-Mv8130_provenance.
- befree-2016 importedOn "2016-02-19" NP480360.RAP88-naLpWtb5SWZW_CtZ8nk_e6ryTH56xxu9Fww-Mv8130_provenance.