Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP196209.RABjJFDV8BMFGEMQg0XVI261m1Wy5T5UD_jr9N-L8U1uU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP196209.RABjJFDV8BMFGEMQg0XVI261m1Wy5T5UD_jr9N-L8U1uU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP196209.RABjJFDV8BMFGEMQg0XVI261m1Wy5T5UD_jr9N-L8U1uU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP196209.RABjJFDV8BMFGEMQg0XVI261m1Wy5T5UD_jr9N-L8U1uU130_provenance.
- NP196209.RABjJFDV8BMFGEMQg0XVI261m1Wy5T5UD_jr9N-L8U1uU130_assertion description "[Several years ago, we described two patients with infantile seizures, delayed development and acquired microcephaly who have normal circulating blood glucose, low-to-normal cerebrospinal fluid (CSF) lactate, but persistent hypoglycorrachia (low CSF glucose) and diminished transport of hexose into isolated red blood cells (RBC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP196209.RABjJFDV8BMFGEMQg0XVI261m1Wy5T5UD_jr9N-L8U1uU130_provenance.
- NP196209.RABjJFDV8BMFGEMQg0XVI261m1Wy5T5UD_jr9N-L8U1uU130_assertion evidence source_evidence_literature NP196209.RABjJFDV8BMFGEMQg0XVI261m1Wy5T5UD_jr9N-L8U1uU130_provenance.
- NP196209.RABjJFDV8BMFGEMQg0XVI261m1Wy5T5UD_jr9N-L8U1uU130_assertion SIO_000772 9462754 NP196209.RABjJFDV8BMFGEMQg0XVI261m1Wy5T5UD_jr9N-L8U1uU130_provenance.
- NP196209.RABjJFDV8BMFGEMQg0XVI261m1Wy5T5UD_jr9N-L8U1uU130_assertion wasDerivedFrom befree-20140225 NP196209.RABjJFDV8BMFGEMQg0XVI261m1Wy5T5UD_jr9N-L8U1uU130_provenance.
- NP196209.RABjJFDV8BMFGEMQg0XVI261m1Wy5T5UD_jr9N-L8U1uU130_assertion wasGeneratedBy ECO_0000203 NP196209.RABjJFDV8BMFGEMQg0XVI261m1Wy5T5UD_jr9N-L8U1uU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP196209.RABjJFDV8BMFGEMQg0XVI261m1Wy5T5UD_jr9N-L8U1uU130_provenance.