Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP720391.RAtzgu9NcNnbV9T6ZukMF70vrvILzXLILEnVyeump-Pmc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP720391.RAtzgu9NcNnbV9T6ZukMF70vrvILzXLILEnVyeump-Pmc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP720391.RAtzgu9NcNnbV9T6ZukMF70vrvILzXLILEnVyeump-Pmc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP720391.RAtzgu9NcNnbV9T6ZukMF70vrvILzXLILEnVyeump-Pmc130_provenance.
- NP720391.RAtzgu9NcNnbV9T6ZukMF70vrvILzXLILEnVyeump-Pmc130_assertion description "[Here, we report a case of diabetes in a 7-mo old child with compound heterozygous mutations in ABCC8 (SUR1[A30V] and SUR1[G296R]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP720391.RAtzgu9NcNnbV9T6ZukMF70vrvILzXLILEnVyeump-Pmc130_provenance.
- NP720391.RAtzgu9NcNnbV9T6ZukMF70vrvILzXLILEnVyeump-Pmc130_assertion evidence source_evidence_literature NP720391.RAtzgu9NcNnbV9T6ZukMF70vrvILzXLILEnVyeump-Pmc130_provenance.
- NP720391.RAtzgu9NcNnbV9T6ZukMF70vrvILzXLILEnVyeump-Pmc130_assertion SIO_000772 22562119 NP720391.RAtzgu9NcNnbV9T6ZukMF70vrvILzXLILEnVyeump-Pmc130_provenance.
- NP720391.RAtzgu9NcNnbV9T6ZukMF70vrvILzXLILEnVyeump-Pmc130_assertion wasDerivedFrom befree-20150227 NP720391.RAtzgu9NcNnbV9T6ZukMF70vrvILzXLILEnVyeump-Pmc130_provenance.
- NP720391.RAtzgu9NcNnbV9T6ZukMF70vrvILzXLILEnVyeump-Pmc130_assertion wasGeneratedBy ECO_0000203 NP720391.RAtzgu9NcNnbV9T6ZukMF70vrvILzXLILEnVyeump-Pmc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP720391.RAtzgu9NcNnbV9T6ZukMF70vrvILzXLILEnVyeump-Pmc130_provenance.