Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP604243.RAULdrX-j4RGZvzn3fYMHSbKWdnFLTZLULMa5d8Ec9qwo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP604243.RAULdrX-j4RGZvzn3fYMHSbKWdnFLTZLULMa5d8Ec9qwo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP604243.RAULdrX-j4RGZvzn3fYMHSbKWdnFLTZLULMa5d8Ec9qwo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP604243.RAULdrX-j4RGZvzn3fYMHSbKWdnFLTZLULMa5d8Ec9qwo130_provenance.
- NP604243.RAULdrX-j4RGZvzn3fYMHSbKWdnFLTZLULMa5d8Ec9qwo130_assertion description "[Branchiootorenal syndrome and oculoauriculovertebral spectrum features associated with duplication of SIX1, SIX6, and OTX2 resulting from a complex chromosomal rearrangement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP604243.RAULdrX-j4RGZvzn3fYMHSbKWdnFLTZLULMa5d8Ec9qwo130_provenance.
- NP604243.RAULdrX-j4RGZvzn3fYMHSbKWdnFLTZLULMa5d8Ec9qwo130_assertion evidence source_evidence_literature NP604243.RAULdrX-j4RGZvzn3fYMHSbKWdnFLTZLULMa5d8Ec9qwo130_provenance.
- NP604243.RAULdrX-j4RGZvzn3fYMHSbKWdnFLTZLULMa5d8Ec9qwo130_assertion SIO_000772 18666230 NP604243.RAULdrX-j4RGZvzn3fYMHSbKWdnFLTZLULMa5d8Ec9qwo130_provenance.
- NP604243.RAULdrX-j4RGZvzn3fYMHSbKWdnFLTZLULMa5d8Ec9qwo130_assertion wasDerivedFrom befree-20150227 NP604243.RAULdrX-j4RGZvzn3fYMHSbKWdnFLTZLULMa5d8Ec9qwo130_provenance.
- NP604243.RAULdrX-j4RGZvzn3fYMHSbKWdnFLTZLULMa5d8Ec9qwo130_assertion wasGeneratedBy ECO_0000203 NP604243.RAULdrX-j4RGZvzn3fYMHSbKWdnFLTZLULMa5d8Ec9qwo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP604243.RAULdrX-j4RGZvzn3fYMHSbKWdnFLTZLULMa5d8Ec9qwo130_provenance.