Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1215295.RAZUm4KC2K8lmw_V9oQmKrmeMDvEGVA1T9T5EQ9k1mtNs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1215295.RAZUm4KC2K8lmw_V9oQmKrmeMDvEGVA1T9T5EQ9k1mtNs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1215295.RAZUm4KC2K8lmw_V9oQmKrmeMDvEGVA1T9T5EQ9k1mtNs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1215295.RAZUm4KC2K8lmw_V9oQmKrmeMDvEGVA1T9T5EQ9k1mtNs130_provenance.
- NP1215295.RAZUm4KC2K8lmw_V9oQmKrmeMDvEGVA1T9T5EQ9k1mtNs130_assertion description "[Our clinical findings are consistent with recessive ECEL1 mutations causing variably penetrant orbital dysinnervation phenotypes (ptosis and/or complex strabismus with abnormal synkinesis) in the context of arthrogryposisis, that is, with the ECEL1-related ophthalmic phenotype being a form of CCDD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1215295.RAZUm4KC2K8lmw_V9oQmKrmeMDvEGVA1T9T5EQ9k1mtNs130_provenance.
- NP1215295.RAZUm4KC2K8lmw_V9oQmKrmeMDvEGVA1T9T5EQ9k1mtNs130_assertion evidence source_evidence_literature NP1215295.RAZUm4KC2K8lmw_V9oQmKrmeMDvEGVA1T9T5EQ9k1mtNs130_provenance.
- NP1215295.RAZUm4KC2K8lmw_V9oQmKrmeMDvEGVA1T9T5EQ9k1mtNs130_assertion SIO_000772 25173900 NP1215295.RAZUm4KC2K8lmw_V9oQmKrmeMDvEGVA1T9T5EQ9k1mtNs130_provenance.
- NP1215295.RAZUm4KC2K8lmw_V9oQmKrmeMDvEGVA1T9T5EQ9k1mtNs130_assertion wasDerivedFrom befree-2016 NP1215295.RAZUm4KC2K8lmw_V9oQmKrmeMDvEGVA1T9T5EQ9k1mtNs130_provenance.
- NP1215295.RAZUm4KC2K8lmw_V9oQmKrmeMDvEGVA1T9T5EQ9k1mtNs130_assertion wasGeneratedBy ECO_0000203 NP1215295.RAZUm4KC2K8lmw_V9oQmKrmeMDvEGVA1T9T5EQ9k1mtNs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1215295.RAZUm4KC2K8lmw_V9oQmKrmeMDvEGVA1T9T5EQ9k1mtNs130_provenance.