Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP226591.RAbIJ_CPdB5dXN_FLoCzsu8v7lR2dqy-iKWJGkk6hw6s0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP226591.RAbIJ_CPdB5dXN_FLoCzsu8v7lR2dqy-iKWJGkk6hw6s0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP226591.RAbIJ_CPdB5dXN_FLoCzsu8v7lR2dqy-iKWJGkk6hw6s0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP226591.RAbIJ_CPdB5dXN_FLoCzsu8v7lR2dqy-iKWJGkk6hw6s0130_provenance.
- NP226591.RAbIJ_CPdB5dXN_FLoCzsu8v7lR2dqy-iKWJGkk6hw6s0130_assertion description "[Thus, GLUD1 mutations can be a cause of congenital hyperinsulinism in Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226591.RAbIJ_CPdB5dXN_FLoCzsu8v7lR2dqy-iKWJGkk6hw6s0130_provenance.
- NP226591.RAbIJ_CPdB5dXN_FLoCzsu8v7lR2dqy-iKWJGkk6hw6s0130_assertion evidence source_evidence_literature NP226591.RAbIJ_CPdB5dXN_FLoCzsu8v7lR2dqy-iKWJGkk6hw6s0130_provenance.
- NP226591.RAbIJ_CPdB5dXN_FLoCzsu8v7lR2dqy-iKWJGkk6hw6s0130_assertion SIO_000772 11201367 NP226591.RAbIJ_CPdB5dXN_FLoCzsu8v7lR2dqy-iKWJGkk6hw6s0130_provenance.
- NP226591.RAbIJ_CPdB5dXN_FLoCzsu8v7lR2dqy-iKWJGkk6hw6s0130_assertion wasDerivedFrom befree-20140225 NP226591.RAbIJ_CPdB5dXN_FLoCzsu8v7lR2dqy-iKWJGkk6hw6s0130_provenance.
- NP226591.RAbIJ_CPdB5dXN_FLoCzsu8v7lR2dqy-iKWJGkk6hw6s0130_assertion wasGeneratedBy ECO_0000203 NP226591.RAbIJ_CPdB5dXN_FLoCzsu8v7lR2dqy-iKWJGkk6hw6s0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP226591.RAbIJ_CPdB5dXN_FLoCzsu8v7lR2dqy-iKWJGkk6hw6s0130_provenance.