Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP602134.RAhtBsq9AICgTX_z6pXlZz2UUzkA3m9sj_CfacGdnKT6U130_assertion> ?p ?o ?g. }
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- NP602134.RAhtBsq9AICgTX_z6pXlZz2UUzkA3m9sj_CfacGdnKT6U130_assertion type Assertion NP602134.RAhtBsq9AICgTX_z6pXlZz2UUzkA3m9sj_CfacGdnKT6U130_head.
- NP602134.RAhtBsq9AICgTX_z6pXlZz2UUzkA3m9sj_CfacGdnKT6U130_assertion description "[Mutations in eight genes (ABCC8, KCNJ11, GLUD1, GCK, HADH, SLC16A1, HNF4A and HNF1A) are known to cause CHI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP602134.RAhtBsq9AICgTX_z6pXlZz2UUzkA3m9sj_CfacGdnKT6U130_provenance.
- NP602134.RAhtBsq9AICgTX_z6pXlZz2UUzkA3m9sj_CfacGdnKT6U130_assertion evidence source_evidence_literature NP602134.RAhtBsq9AICgTX_z6pXlZz2UUzkA3m9sj_CfacGdnKT6U130_provenance.
- NP602134.RAhtBsq9AICgTX_z6pXlZz2UUzkA3m9sj_CfacGdnKT6U130_assertion SIO_000772 23345197 NP602134.RAhtBsq9AICgTX_z6pXlZz2UUzkA3m9sj_CfacGdnKT6U130_provenance.
- NP602134.RAhtBsq9AICgTX_z6pXlZz2UUzkA3m9sj_CfacGdnKT6U130_assertion wasDerivedFrom befree-20140225 NP602134.RAhtBsq9AICgTX_z6pXlZz2UUzkA3m9sj_CfacGdnKT6U130_provenance.
- NP602134.RAhtBsq9AICgTX_z6pXlZz2UUzkA3m9sj_CfacGdnKT6U130_assertion wasGeneratedBy ECO_0000203 NP602134.RAhtBsq9AICgTX_z6pXlZz2UUzkA3m9sj_CfacGdnKT6U130_provenance.