Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP546938.RAYnqhpeJ1EvBCzNOa6tYYmmoXbS_pHQYFgq3BNPzjXCk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP546938.RAYnqhpeJ1EvBCzNOa6tYYmmoXbS_pHQYFgq3BNPzjXCk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP546938.RAYnqhpeJ1EvBCzNOa6tYYmmoXbS_pHQYFgq3BNPzjXCk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP546938.RAYnqhpeJ1EvBCzNOa6tYYmmoXbS_pHQYFgq3BNPzjXCk130_provenance.
- NP546938.RAYnqhpeJ1EvBCzNOa6tYYmmoXbS_pHQYFgq3BNPzjXCk130_assertion description "[Cases 3 and 4, two siblings with a novel variant in ARX, which is not clearly pathogenic, have developmental delay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP546938.RAYnqhpeJ1EvBCzNOa6tYYmmoXbS_pHQYFgq3BNPzjXCk130_provenance.
- NP546938.RAYnqhpeJ1EvBCzNOa6tYYmmoXbS_pHQYFgq3BNPzjXCk130_assertion evidence source_evidence_literature NP546938.RAYnqhpeJ1EvBCzNOa6tYYmmoXbS_pHQYFgq3BNPzjXCk130_provenance.
- NP546938.RAYnqhpeJ1EvBCzNOa6tYYmmoXbS_pHQYFgq3BNPzjXCk130_assertion SIO_000772 18462864 NP546938.RAYnqhpeJ1EvBCzNOa6tYYmmoXbS_pHQYFgq3BNPzjXCk130_provenance.
- NP546938.RAYnqhpeJ1EvBCzNOa6tYYmmoXbS_pHQYFgq3BNPzjXCk130_assertion wasDerivedFrom befree-20140225 NP546938.RAYnqhpeJ1EvBCzNOa6tYYmmoXbS_pHQYFgq3BNPzjXCk130_provenance.
- NP546938.RAYnqhpeJ1EvBCzNOa6tYYmmoXbS_pHQYFgq3BNPzjXCk130_assertion wasGeneratedBy ECO_0000203 NP546938.RAYnqhpeJ1EvBCzNOa6tYYmmoXbS_pHQYFgq3BNPzjXCk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP546938.RAYnqhpeJ1EvBCzNOa6tYYmmoXbS_pHQYFgq3BNPzjXCk130_provenance.