Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP280262.RAslOGXfWnp7gBhVRv2zIvVgs24ocHQPcwYpXay8woT-Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP280262.RAslOGXfWnp7gBhVRv2zIvVgs24ocHQPcwYpXay8woT-Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP280262.RAslOGXfWnp7gBhVRv2zIvVgs24ocHQPcwYpXay8woT-Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP280262.RAslOGXfWnp7gBhVRv2zIvVgs24ocHQPcwYpXay8woT-Q130_provenance.
- NP280262.RAslOGXfWnp7gBhVRv2zIvVgs24ocHQPcwYpXay8woT-Q130_assertion description "[Characterization of ABCC8 and KCNJ11 gene mutations and phenotypes in Korean patients with congenital hyperinsulinism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280262.RAslOGXfWnp7gBhVRv2zIvVgs24ocHQPcwYpXay8woT-Q130_provenance.
- NP280262.RAslOGXfWnp7gBhVRv2zIvVgs24ocHQPcwYpXay8woT-Q130_assertion evidence source_evidence_literature NP280262.RAslOGXfWnp7gBhVRv2zIvVgs24ocHQPcwYpXay8woT-Q130_provenance.
- NP280262.RAslOGXfWnp7gBhVRv2zIvVgs24ocHQPcwYpXay8woT-Q130_assertion SIO_000772 21422196 NP280262.RAslOGXfWnp7gBhVRv2zIvVgs24ocHQPcwYpXay8woT-Q130_provenance.
- NP280262.RAslOGXfWnp7gBhVRv2zIvVgs24ocHQPcwYpXay8woT-Q130_assertion wasDerivedFrom befree-20140225 NP280262.RAslOGXfWnp7gBhVRv2zIvVgs24ocHQPcwYpXay8woT-Q130_provenance.
- NP280262.RAslOGXfWnp7gBhVRv2zIvVgs24ocHQPcwYpXay8woT-Q130_assertion wasGeneratedBy ECO_0000203 NP280262.RAslOGXfWnp7gBhVRv2zIvVgs24ocHQPcwYpXay8woT-Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP280262.RAslOGXfWnp7gBhVRv2zIvVgs24ocHQPcwYpXay8woT-Q130_provenance.