Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP600515.RA5ANr6MLyMGHoPaYWWWCfuspFzpfeSfFvjL66UgZl3hA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP600515.RA5ANr6MLyMGHoPaYWWWCfuspFzpfeSfFvjL66UgZl3hA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP600515.RA5ANr6MLyMGHoPaYWWWCfuspFzpfeSfFvjL66UgZl3hA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP600515.RA5ANr6MLyMGHoPaYWWWCfuspFzpfeSfFvjL66UgZl3hA130_provenance.
- NP600515.RA5ANr6MLyMGHoPaYWWWCfuspFzpfeSfFvjL66UgZl3hA130_assertion description "[Here we report the identification of two novel mutations in the frizzled-like cysteine-rich domain of ROR2 causing Robinow syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600515.RA5ANr6MLyMGHoPaYWWWCfuspFzpfeSfFvjL66UgZl3hA130_provenance.
- NP600515.RA5ANr6MLyMGHoPaYWWWCfuspFzpfeSfFvjL66UgZl3hA130_assertion evidence source_evidence_literature NP600515.RA5ANr6MLyMGHoPaYWWWCfuspFzpfeSfFvjL66UgZl3hA130_provenance.
- NP600515.RA5ANr6MLyMGHoPaYWWWCfuspFzpfeSfFvjL66UgZl3hA130_assertion SIO_000772 17665217 NP600515.RA5ANr6MLyMGHoPaYWWWCfuspFzpfeSfFvjL66UgZl3hA130_provenance.
- NP600515.RA5ANr6MLyMGHoPaYWWWCfuspFzpfeSfFvjL66UgZl3hA130_assertion wasDerivedFrom befree-20150227 NP600515.RA5ANr6MLyMGHoPaYWWWCfuspFzpfeSfFvjL66UgZl3hA130_provenance.
- NP600515.RA5ANr6MLyMGHoPaYWWWCfuspFzpfeSfFvjL66UgZl3hA130_assertion wasGeneratedBy ECO_0000203 NP600515.RA5ANr6MLyMGHoPaYWWWCfuspFzpfeSfFvjL66UgZl3hA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP600515.RA5ANr6MLyMGHoPaYWWWCfuspFzpfeSfFvjL66UgZl3hA130_provenance.