Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP769944.RAD5_0ycuohnvPy4hMqkZENwsMGCU8RtHjRnevpmJDV2g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP769944.RAD5_0ycuohnvPy4hMqkZENwsMGCU8RtHjRnevpmJDV2g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP769944.RAD5_0ycuohnvPy4hMqkZENwsMGCU8RtHjRnevpmJDV2g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP769944.RAD5_0ycuohnvPy4hMqkZENwsMGCU8RtHjRnevpmJDV2g130_provenance.
- NP769944.RAD5_0ycuohnvPy4hMqkZENwsMGCU8RtHjRnevpmJDV2g130_assertion description "[In contrast to nonconsanguineous pedigrees, mutations in EIF2AK3 are the most common known genetic cause of diabetes among patients born to consanguineous parents (24 vs. < 2%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP769944.RAD5_0ycuohnvPy4hMqkZENwsMGCU8RtHjRnevpmJDV2g130_provenance.
- NP769944.RAD5_0ycuohnvPy4hMqkZENwsMGCU8RtHjRnevpmJDV2g130_assertion evidence source_evidence_literature NP769944.RAD5_0ycuohnvPy4hMqkZENwsMGCU8RtHjRnevpmJDV2g130_provenance.
- NP769944.RAD5_0ycuohnvPy4hMqkZENwsMGCU8RtHjRnevpmJDV2g130_assertion SIO_000772 19837917 NP769944.RAD5_0ycuohnvPy4hMqkZENwsMGCU8RtHjRnevpmJDV2g130_provenance.
- NP769944.RAD5_0ycuohnvPy4hMqkZENwsMGCU8RtHjRnevpmJDV2g130_assertion wasDerivedFrom befree-2016 NP769944.RAD5_0ycuohnvPy4hMqkZENwsMGCU8RtHjRnevpmJDV2g130_provenance.
- NP769944.RAD5_0ycuohnvPy4hMqkZENwsMGCU8RtHjRnevpmJDV2g130_assertion wasGeneratedBy ECO_0000203 NP769944.RAD5_0ycuohnvPy4hMqkZENwsMGCU8RtHjRnevpmJDV2g130_provenance.
- befree-2016 importedOn "2016-02-19" NP769944.RAD5_0ycuohnvPy4hMqkZENwsMGCU8RtHjRnevpmJDV2g130_provenance.