Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP12546.RAG0SebBjY2xV2hfumn-iD-Ipv5kmRqQ_KZh1RzI-ALhU130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP12546.RAG0SebBjY2xV2hfumn-iD-Ipv5kmRqQ_KZh1RzI-ALhU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP12546.RAG0SebBjY2xV2hfumn-iD-Ipv5kmRqQ_KZh1RzI-ALhU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP12546.RAG0SebBjY2xV2hfumn-iD-Ipv5kmRqQ_KZh1RzI-ALhU130_provenance.
- NP12546.RAG0SebBjY2xV2hfumn-iD-Ipv5kmRqQ_KZh1RzI-ALhU130_assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP12546.RAG0SebBjY2xV2hfumn-iD-Ipv5kmRqQ_KZh1RzI-ALhU130_provenance.
- NP12546.RAG0SebBjY2xV2hfumn-iD-Ipv5kmRqQ_KZh1RzI-ALhU130_assertion evidence source_evidence_curated NP12546.RAG0SebBjY2xV2hfumn-iD-Ipv5kmRqQ_KZh1RzI-ALhU130_provenance.
- NP12546.RAG0SebBjY2xV2hfumn-iD-Ipv5kmRqQ_KZh1RzI-ALhU130_assertion SIO_000772 11389483 NP12546.RAG0SebBjY2xV2hfumn-iD-Ipv5kmRqQ_KZh1RzI-ALhU130_provenance.
- NP12546.RAG0SebBjY2xV2hfumn-iD-Ipv5kmRqQ_KZh1RzI-ALhU130_assertion wasDerivedFrom ctd_human-20130708 NP12546.RAG0SebBjY2xV2hfumn-iD-Ipv5kmRqQ_KZh1RzI-ALhU130_provenance.
- NP12546.RAG0SebBjY2xV2hfumn-iD-Ipv5kmRqQ_KZh1RzI-ALhU130_assertion wasGeneratedBy ECO_0000218 NP12546.RAG0SebBjY2xV2hfumn-iD-Ipv5kmRqQ_KZh1RzI-ALhU130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP12546.RAG0SebBjY2xV2hfumn-iD-Ipv5kmRqQ_KZh1RzI-ALhU130_provenance.