Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP877767.RAoBFf6ztDVW7h7ZcgcBsT8VvsYqTGrhIpXMC6lcJaK3I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP877767.RAoBFf6ztDVW7h7ZcgcBsT8VvsYqTGrhIpXMC6lcJaK3I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP877767.RAoBFf6ztDVW7h7ZcgcBsT8VvsYqTGrhIpXMC6lcJaK3I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP877767.RAoBFf6ztDVW7h7ZcgcBsT8VvsYqTGrhIpXMC6lcJaK3I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP877767.RAoBFf6ztDVW7h7ZcgcBsT8VvsYqTGrhIpXMC6lcJaK3I130_provenance.
- NP877767.RAoBFf6ztDVW7h7ZcgcBsT8VvsYqTGrhIpXMC6lcJaK3I130_assertion wasGeneratedBy ECO_0000203 NP877767.RAoBFf6ztDVW7h7ZcgcBsT8VvsYqTGrhIpXMC6lcJaK3I130_provenance.
- NP877767.RAoBFf6ztDVW7h7ZcgcBsT8VvsYqTGrhIpXMC6lcJaK3I130_assertion wasDerivedFrom befree-20150227 NP877767.RAoBFf6ztDVW7h7ZcgcBsT8VvsYqTGrhIpXMC6lcJaK3I130_provenance.
- NP877767.RAoBFf6ztDVW7h7ZcgcBsT8VvsYqTGrhIpXMC6lcJaK3I130_assertion SIO_000772 20967465 NP877767.RAoBFf6ztDVW7h7ZcgcBsT8VvsYqTGrhIpXMC6lcJaK3I130_provenance.
- NP877767.RAoBFf6ztDVW7h7ZcgcBsT8VvsYqTGrhIpXMC6lcJaK3I130_assertion evidence source_evidence_literature NP877767.RAoBFf6ztDVW7h7ZcgcBsT8VvsYqTGrhIpXMC6lcJaK3I130_provenance.
- NP877767.RAoBFf6ztDVW7h7ZcgcBsT8VvsYqTGrhIpXMC6lcJaK3I130_assertion description "[Here, we report a novel homozygous RAB3GAP2 small in-frame deletion, c.499_507delTTCTACACT (p.Phe167_Thr169del) that causes Warburg Micro syndrome in a girl from a consanguineous Turkish family presenting with congenital cataracts, microphthalmia, absent visually evoked potentials, microcephaly, polymicrogyria, hypoplasia of the corpus callosum, and severe developmental delay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP877767.RAoBFf6ztDVW7h7ZcgcBsT8VvsYqTGrhIpXMC6lcJaK3I130_provenance.