Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP4958.RA7ZLr8D5ZaN6mCjeC_ZdKU2img9djZTnuK9LLM3yrhzY130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4958.RA7ZLr8D5ZaN6mCjeC_ZdKU2img9djZTnuK9LLM3yrhzY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4958.RA7ZLr8D5ZaN6mCjeC_ZdKU2img9djZTnuK9LLM3yrhzY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4958.RA7ZLr8D5ZaN6mCjeC_ZdKU2img9djZTnuK9LLM3yrhzY130_provenance.
- NP4958.RA7ZLr8D5ZaN6mCjeC_ZdKU2img9djZTnuK9LLM3yrhzY130_assertion description "[Functional analyses of two newly identified PITX2 mutants reveal a novel molecular mechanism for Axenfeld-Rieger syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4958.RA7ZLr8D5ZaN6mCjeC_ZdKU2img9djZTnuK9LLM3yrhzY130_provenance.
- NP4958.RA7ZLr8D5ZaN6mCjeC_ZdKU2img9djZTnuK9LLM3yrhzY130_assertion evidence source_evidence_curated NP4958.RA7ZLr8D5ZaN6mCjeC_ZdKU2img9djZTnuK9LLM3yrhzY130_provenance.
- NP4958.RA7ZLr8D5ZaN6mCjeC_ZdKU2img9djZTnuK9LLM3yrhzY130_assertion SIO_000772 11487566 NP4958.RA7ZLr8D5ZaN6mCjeC_ZdKU2img9djZTnuK9LLM3yrhzY130_provenance.
- NP4958.RA7ZLr8D5ZaN6mCjeC_ZdKU2img9djZTnuK9LLM3yrhzY130_assertion wasDerivedFrom uniprot-20130724 NP4958.RA7ZLr8D5ZaN6mCjeC_ZdKU2img9djZTnuK9LLM3yrhzY130_provenance.
- NP4958.RA7ZLr8D5ZaN6mCjeC_ZdKU2img9djZTnuK9LLM3yrhzY130_assertion wasGeneratedBy ECO_0000218 NP4958.RA7ZLr8D5ZaN6mCjeC_ZdKU2img9djZTnuK9LLM3yrhzY130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP4958.RA7ZLr8D5ZaN6mCjeC_ZdKU2img9djZTnuK9LLM3yrhzY130_provenance.