Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP429053.RAQwjHKdO633qDLvprZjuXOWe5ihpq_2BqTww6UvXrP44130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP429053.RAQwjHKdO633qDLvprZjuXOWe5ihpq_2BqTww6UvXrP44130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP429053.RAQwjHKdO633qDLvprZjuXOWe5ihpq_2BqTww6UvXrP44130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP429053.RAQwjHKdO633qDLvprZjuXOWe5ihpq_2BqTww6UvXrP44130_provenance.
- NP429053.RAQwjHKdO633qDLvprZjuXOWe5ihpq_2BqTww6UvXrP44130_assertion description "[Hyperinsulinism-hyperammonemia syndrome (HI/HA) (OMIM 606762), the second most common form of congenital hyperinsulinism (CHI) is associated with activating missense mutations in the GLUD1 gene, which encodes the mitochondrial matrix enzyme, glutamate dehydrogenase (GDH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429053.RAQwjHKdO633qDLvprZjuXOWe5ihpq_2BqTww6UvXrP44130_provenance.
- NP429053.RAQwjHKdO633qDLvprZjuXOWe5ihpq_2BqTww6UvXrP44130_assertion evidence source_evidence_literature NP429053.RAQwjHKdO633qDLvprZjuXOWe5ihpq_2BqTww6UvXrP44130_provenance.
- NP429053.RAQwjHKdO633qDLvprZjuXOWe5ihpq_2BqTww6UvXrP44130_assertion SIO_000772 21932603 NP429053.RAQwjHKdO633qDLvprZjuXOWe5ihpq_2BqTww6UvXrP44130_provenance.
- NP429053.RAQwjHKdO633qDLvprZjuXOWe5ihpq_2BqTww6UvXrP44130_assertion wasDerivedFrom befree-20150227 NP429053.RAQwjHKdO633qDLvprZjuXOWe5ihpq_2BqTww6UvXrP44130_provenance.
- NP429053.RAQwjHKdO633qDLvprZjuXOWe5ihpq_2BqTww6UvXrP44130_assertion wasGeneratedBy ECO_0000203 NP429053.RAQwjHKdO633qDLvprZjuXOWe5ihpq_2BqTww6UvXrP44130_provenance.
- befree-20150227 importedOn "2015-02-27" NP429053.RAQwjHKdO633qDLvprZjuXOWe5ihpq_2BqTww6UvXrP44130_provenance.