Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP692129.RAILSv318GAkUpegFzid5WJ2-e0qeuPGiPWUjlUkjn3Jo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP692129.RAILSv318GAkUpegFzid5WJ2-e0qeuPGiPWUjlUkjn3Jo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP692129.RAILSv318GAkUpegFzid5WJ2-e0qeuPGiPWUjlUkjn3Jo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP692129.RAILSv318GAkUpegFzid5WJ2-e0qeuPGiPWUjlUkjn3Jo130_provenance.
- NP692129.RAILSv318GAkUpegFzid5WJ2-e0qeuPGiPWUjlUkjn3Jo130_assertion description "[Patients and methods Twenty patients with HI from 16 families had mutational analysis of the GLUD1 gene in view of HA (n=19) or leucine sensitivity (n=1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692129.RAILSv318GAkUpegFzid5WJ2-e0qeuPGiPWUjlUkjn3Jo130_provenance.
- NP692129.RAILSv318GAkUpegFzid5WJ2-e0qeuPGiPWUjlUkjn3Jo130_assertion evidence source_evidence_literature NP692129.RAILSv318GAkUpegFzid5WJ2-e0qeuPGiPWUjlUkjn3Jo130_provenance.
- NP692129.RAILSv318GAkUpegFzid5WJ2-e0qeuPGiPWUjlUkjn3Jo130_assertion SIO_000772 19690084 NP692129.RAILSv318GAkUpegFzid5WJ2-e0qeuPGiPWUjlUkjn3Jo130_provenance.
- NP692129.RAILSv318GAkUpegFzid5WJ2-e0qeuPGiPWUjlUkjn3Jo130_assertion wasDerivedFrom befree-20140225 NP692129.RAILSv318GAkUpegFzid5WJ2-e0qeuPGiPWUjlUkjn3Jo130_provenance.
- NP692129.RAILSv318GAkUpegFzid5WJ2-e0qeuPGiPWUjlUkjn3Jo130_assertion wasGeneratedBy ECO_0000203 NP692129.RAILSv318GAkUpegFzid5WJ2-e0qeuPGiPWUjlUkjn3Jo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP692129.RAILSv318GAkUpegFzid5WJ2-e0qeuPGiPWUjlUkjn3Jo130_provenance.