Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP19502.RAeSDLP5NpYRZm8bexSBs3aglRgfQjceP3NIQKHxRmbQU130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP19502.RAeSDLP5NpYRZm8bexSBs3aglRgfQjceP3NIQKHxRmbQU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP19502.RAeSDLP5NpYRZm8bexSBs3aglRgfQjceP3NIQKHxRmbQU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP19502.RAeSDLP5NpYRZm8bexSBs3aglRgfQjceP3NIQKHxRmbQU130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP19502.RAeSDLP5NpYRZm8bexSBs3aglRgfQjceP3NIQKHxRmbQU130_provenance.
- 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.