Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP19502.RAeSDLP5NpYRZm8bexSBs3aglRgfQjceP3NIQKHxRmbQU130_assertion> ?p ?o ?g. }
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- NP19502.RAeSDLP5NpYRZm8bexSBs3aglRgfQjceP3NIQKHxRmbQU130_assertion type Assertion NP19502.RAeSDLP5NpYRZm8bexSBs3aglRgfQjceP3NIQKHxRmbQU130_head.
- NP19502.RAeSDLP5NpYRZm8bexSBs3aglRgfQjceP3NIQKHxRmbQU130_assertion wasGeneratedBy ECO_0000218 NP19502.RAeSDLP5NpYRZm8bexSBs3aglRgfQjceP3NIQKHxRmbQU130_provenance.
- NP19502.RAeSDLP5NpYRZm8bexSBs3aglRgfQjceP3NIQKHxRmbQU130_assertion wasDerivedFrom ctd_human-20150221 NP19502.RAeSDLP5NpYRZm8bexSBs3aglRgfQjceP3NIQKHxRmbQU130_provenance.
- NP19502.RAeSDLP5NpYRZm8bexSBs3aglRgfQjceP3NIQKHxRmbQU130_assertion SIO_000772 18162506 NP19502.RAeSDLP5NpYRZm8bexSBs3aglRgfQjceP3NIQKHxRmbQU130_provenance.
- NP19502.RAeSDLP5NpYRZm8bexSBs3aglRgfQjceP3NIQKHxRmbQU130_assertion evidence source_evidence_curated NP19502.RAeSDLP5NpYRZm8bexSBs3aglRgfQjceP3NIQKHxRmbQU130_provenance.
- NP19502.RAeSDLP5NpYRZm8bexSBs3aglRgfQjceP3NIQKHxRmbQU130_assertion description "[Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP19502.RAeSDLP5NpYRZm8bexSBs3aglRgfQjceP3NIQKHxRmbQU130_provenance.