Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP188022.RArfwxorav7Po1KwCCaQZxfBbz_JgVn1PlmFit33OxBnU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP188022.RArfwxorav7Po1KwCCaQZxfBbz_JgVn1PlmFit33OxBnU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP188022.RArfwxorav7Po1KwCCaQZxfBbz_JgVn1PlmFit33OxBnU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP188022.RArfwxorav7Po1KwCCaQZxfBbz_JgVn1PlmFit33OxBnU130_provenance.
- NP188022.RArfwxorav7Po1KwCCaQZxfBbz_JgVn1PlmFit33OxBnU130_assertion description "[Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188022.RArfwxorav7Po1KwCCaQZxfBbz_JgVn1PlmFit33OxBnU130_provenance.
- NP188022.RArfwxorav7Po1KwCCaQZxfBbz_JgVn1PlmFit33OxBnU130_assertion evidence source_evidence_literature NP188022.RArfwxorav7Po1KwCCaQZxfBbz_JgVn1PlmFit33OxBnU130_provenance.
- NP188022.RArfwxorav7Po1KwCCaQZxfBbz_JgVn1PlmFit33OxBnU130_assertion SIO_000772 9719369 NP188022.RArfwxorav7Po1KwCCaQZxfBbz_JgVn1PlmFit33OxBnU130_provenance.
- NP188022.RArfwxorav7Po1KwCCaQZxfBbz_JgVn1PlmFit33OxBnU130_assertion wasDerivedFrom befree-20140225 NP188022.RArfwxorav7Po1KwCCaQZxfBbz_JgVn1PlmFit33OxBnU130_provenance.
- NP188022.RArfwxorav7Po1KwCCaQZxfBbz_JgVn1PlmFit33OxBnU130_assertion wasGeneratedBy ECO_0000203 NP188022.RArfwxorav7Po1KwCCaQZxfBbz_JgVn1PlmFit33OxBnU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP188022.RArfwxorav7Po1KwCCaQZxfBbz_JgVn1PlmFit33OxBnU130_provenance.