Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP719394.RAoTnnsoslPQDrC2GwWQ7MujlLCF_p8HEFbnHtkSRPXoU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP719394.RAoTnnsoslPQDrC2GwWQ7MujlLCF_p8HEFbnHtkSRPXoU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP719394.RAoTnnsoslPQDrC2GwWQ7MujlLCF_p8HEFbnHtkSRPXoU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP719394.RAoTnnsoslPQDrC2GwWQ7MujlLCF_p8HEFbnHtkSRPXoU130_provenance.
- NP719394.RAoTnnsoslPQDrC2GwWQ7MujlLCF_p8HEFbnHtkSRPXoU130_assertion description "[The screening was negative for all men as well as for women with Aicardi syndrome, excluding the CDKL5 gene as a candidate for this neurodevelopmental disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719394.RAoTnnsoslPQDrC2GwWQ7MujlLCF_p8HEFbnHtkSRPXoU130_provenance.
- NP719394.RAoTnnsoslPQDrC2GwWQ7MujlLCF_p8HEFbnHtkSRPXoU130_assertion evidence source_evidence_literature NP719394.RAoTnnsoslPQDrC2GwWQ7MujlLCF_p8HEFbnHtkSRPXoU130_provenance.
- NP719394.RAoTnnsoslPQDrC2GwWQ7MujlLCF_p8HEFbnHtkSRPXoU130_assertion SIO_000772 19793311 NP719394.RAoTnnsoslPQDrC2GwWQ7MujlLCF_p8HEFbnHtkSRPXoU130_provenance.
- NP719394.RAoTnnsoslPQDrC2GwWQ7MujlLCF_p8HEFbnHtkSRPXoU130_assertion wasDerivedFrom befree-20150227 NP719394.RAoTnnsoslPQDrC2GwWQ7MujlLCF_p8HEFbnHtkSRPXoU130_provenance.
- NP719394.RAoTnnsoslPQDrC2GwWQ7MujlLCF_p8HEFbnHtkSRPXoU130_assertion wasGeneratedBy ECO_0000203 NP719394.RAoTnnsoslPQDrC2GwWQ7MujlLCF_p8HEFbnHtkSRPXoU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP719394.RAoTnnsoslPQDrC2GwWQ7MujlLCF_p8HEFbnHtkSRPXoU130_provenance.