Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP584220.RATKRsShWgshElzVUo8M--JaBxrV9GCGXioDbhVCPBkeQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP584220.RATKRsShWgshElzVUo8M--JaBxrV9GCGXioDbhVCPBkeQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584220.RATKRsShWgshElzVUo8M--JaBxrV9GCGXioDbhVCPBkeQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584220.RATKRsShWgshElzVUo8M--JaBxrV9GCGXioDbhVCPBkeQ130_provenance.
- NP584220.RATKRsShWgshElzVUo8M--JaBxrV9GCGXioDbhVCPBkeQ130_assertion description "[The membrane-type frizzled-related protein (MFRP) and CEH10 homeodomain-containing homolog (CHX10) genes, previously implicated in autosomal recessive forms of nanophthalmos/microphthalmos, were analyzed as candidate genes for this novel disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584220.RATKRsShWgshElzVUo8M--JaBxrV9GCGXioDbhVCPBkeQ130_provenance.
- NP584220.RATKRsShWgshElzVUo8M--JaBxrV9GCGXioDbhVCPBkeQ130_assertion evidence source_evidence_literature NP584220.RATKRsShWgshElzVUo8M--JaBxrV9GCGXioDbhVCPBkeQ130_provenance.
- NP584220.RATKRsShWgshElzVUo8M--JaBxrV9GCGXioDbhVCPBkeQ130_assertion SIO_000772 17167404 NP584220.RATKRsShWgshElzVUo8M--JaBxrV9GCGXioDbhVCPBkeQ130_provenance.
- NP584220.RATKRsShWgshElzVUo8M--JaBxrV9GCGXioDbhVCPBkeQ130_assertion wasDerivedFrom befree-2016 NP584220.RATKRsShWgshElzVUo8M--JaBxrV9GCGXioDbhVCPBkeQ130_provenance.
- NP584220.RATKRsShWgshElzVUo8M--JaBxrV9GCGXioDbhVCPBkeQ130_assertion wasGeneratedBy ECO_0000203 NP584220.RATKRsShWgshElzVUo8M--JaBxrV9GCGXioDbhVCPBkeQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP584220.RATKRsShWgshElzVUo8M--JaBxrV9GCGXioDbhVCPBkeQ130_provenance.