Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP881281.RA4t2IHyLMRKPV59qkykHWiDTomp9Tcq0D3Fdk2uDrTu0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP881281.RA4t2IHyLMRKPV59qkykHWiDTomp9Tcq0D3Fdk2uDrTu0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881281.RA4t2IHyLMRKPV59qkykHWiDTomp9Tcq0D3Fdk2uDrTu0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881281.RA4t2IHyLMRKPV59qkykHWiDTomp9Tcq0D3Fdk2uDrTu0130_provenance.
- NP881281.RA4t2IHyLMRKPV59qkykHWiDTomp9Tcq0D3Fdk2uDrTu0130_assertion description "[This study reveals that mutations in the ADAMTS18 gene can cause a broad phenotypic spectrum of eye disorders and contribute to shed further light on the complexity of retinal diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881281.RA4t2IHyLMRKPV59qkykHWiDTomp9Tcq0D3Fdk2uDrTu0130_provenance.
- NP881281.RA4t2IHyLMRKPV59qkykHWiDTomp9Tcq0D3Fdk2uDrTu0130_assertion evidence source_evidence_literature NP881281.RA4t2IHyLMRKPV59qkykHWiDTomp9Tcq0D3Fdk2uDrTu0130_provenance.
- NP881281.RA4t2IHyLMRKPV59qkykHWiDTomp9Tcq0D3Fdk2uDrTu0130_assertion SIO_000772 23356391 NP881281.RA4t2IHyLMRKPV59qkykHWiDTomp9Tcq0D3Fdk2uDrTu0130_provenance.
- NP881281.RA4t2IHyLMRKPV59qkykHWiDTomp9Tcq0D3Fdk2uDrTu0130_assertion wasDerivedFrom befree-20140225 NP881281.RA4t2IHyLMRKPV59qkykHWiDTomp9Tcq0D3Fdk2uDrTu0130_provenance.
- NP881281.RA4t2IHyLMRKPV59qkykHWiDTomp9Tcq0D3Fdk2uDrTu0130_assertion wasGeneratedBy ECO_0000203 NP881281.RA4t2IHyLMRKPV59qkykHWiDTomp9Tcq0D3Fdk2uDrTu0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP881281.RA4t2IHyLMRKPV59qkykHWiDTomp9Tcq0D3Fdk2uDrTu0130_provenance.