Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP715606.RAkSWJDjr0ddNkXrLJSeRlVWZBx6Fz6nWiL3Agyjfoo3c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP715606.RAkSWJDjr0ddNkXrLJSeRlVWZBx6Fz6nWiL3Agyjfoo3c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP715606.RAkSWJDjr0ddNkXrLJSeRlVWZBx6Fz6nWiL3Agyjfoo3c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP715606.RAkSWJDjr0ddNkXrLJSeRlVWZBx6Fz6nWiL3Agyjfoo3c130_provenance.
- NP715606.RAkSWJDjr0ddNkXrLJSeRlVWZBx6Fz6nWiL3Agyjfoo3c130_assertion description "[Biochemical evaluation of an infant with hypoglycemia resulting from a novel de novo mutation of the GLUD1 gene and hyperinsulinism-hyperammonemia syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715606.RAkSWJDjr0ddNkXrLJSeRlVWZBx6Fz6nWiL3Agyjfoo3c130_provenance.
- NP715606.RAkSWJDjr0ddNkXrLJSeRlVWZBx6Fz6nWiL3Agyjfoo3c130_assertion evidence source_evidence_literature NP715606.RAkSWJDjr0ddNkXrLJSeRlVWZBx6Fz6nWiL3Agyjfoo3c130_provenance.
- NP715606.RAkSWJDjr0ddNkXrLJSeRlVWZBx6Fz6nWiL3Agyjfoo3c130_assertion SIO_000772 21932603 NP715606.RAkSWJDjr0ddNkXrLJSeRlVWZBx6Fz6nWiL3Agyjfoo3c130_provenance.
- NP715606.RAkSWJDjr0ddNkXrLJSeRlVWZBx6Fz6nWiL3Agyjfoo3c130_assertion wasDerivedFrom befree-20140225 NP715606.RAkSWJDjr0ddNkXrLJSeRlVWZBx6Fz6nWiL3Agyjfoo3c130_provenance.
- NP715606.RAkSWJDjr0ddNkXrLJSeRlVWZBx6Fz6nWiL3Agyjfoo3c130_assertion wasGeneratedBy ECO_0000203 NP715606.RAkSWJDjr0ddNkXrLJSeRlVWZBx6Fz6nWiL3Agyjfoo3c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP715606.RAkSWJDjr0ddNkXrLJSeRlVWZBx6Fz6nWiL3Agyjfoo3c130_provenance.