Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP769945.RAILQYwNFYmXjiwyRRsL1Nr0u0xJ8x09R85HuEYDu8Ges130_assertion> ?p ?o ?g. }
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- NP769945.RAILQYwNFYmXjiwyRRsL1Nr0u0xJ8x09R85HuEYDu8Ges130_assertion type Assertion NP769945.RAILQYwNFYmXjiwyRRsL1Nr0u0xJ8x09R85HuEYDu8Ges130_head.
- NP769945.RAILQYwNFYmXjiwyRRsL1Nr0u0xJ8x09R85HuEYDu8Ges130_assertion description "[The coding regions of EIF2AK3 were sequenced in 34 probands with infancy-onset diabetes with a clinical phenotype suggestive of WRS (n = 28) or homozygosity at the WRS locus (n = 6).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP769945.RAILQYwNFYmXjiwyRRsL1Nr0u0xJ8x09R85HuEYDu8Ges130_provenance.
- NP769945.RAILQYwNFYmXjiwyRRsL1Nr0u0xJ8x09R85HuEYDu8Ges130_assertion evidence source_evidence_literature NP769945.RAILQYwNFYmXjiwyRRsL1Nr0u0xJ8x09R85HuEYDu8Ges130_provenance.
- NP769945.RAILQYwNFYmXjiwyRRsL1Nr0u0xJ8x09R85HuEYDu8Ges130_assertion SIO_000772 19837917 NP769945.RAILQYwNFYmXjiwyRRsL1Nr0u0xJ8x09R85HuEYDu8Ges130_provenance.
- NP769945.RAILQYwNFYmXjiwyRRsL1Nr0u0xJ8x09R85HuEYDu8Ges130_assertion wasDerivedFrom befree-2016 NP769945.RAILQYwNFYmXjiwyRRsL1Nr0u0xJ8x09R85HuEYDu8Ges130_provenance.
- NP769945.RAILQYwNFYmXjiwyRRsL1Nr0u0xJ8x09R85HuEYDu8Ges130_assertion wasGeneratedBy ECO_0000203 NP769945.RAILQYwNFYmXjiwyRRsL1Nr0u0xJ8x09R85HuEYDu8Ges130_provenance.