Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP177.RAI9vLIMKc1LoI8jOmSkVOAc1IxrtzWyulcjMpEjAAWeo130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP177.RAI9vLIMKc1LoI8jOmSkVOAc1IxrtzWyulcjMpEjAAWeo130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP177.RAI9vLIMKc1LoI8jOmSkVOAc1IxrtzWyulcjMpEjAAWeo130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP177.RAI9vLIMKc1LoI8jOmSkVOAc1IxrtzWyulcjMpEjAAWeo130_provenance.
- NP177.RAI9vLIMKc1LoI8jOmSkVOAc1IxrtzWyulcjMpEjAAWeo130_assertion description "[Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177.RAI9vLIMKc1LoI8jOmSkVOAc1IxrtzWyulcjMpEjAAWeo130_provenance.
- NP177.RAI9vLIMKc1LoI8jOmSkVOAc1IxrtzWyulcjMpEjAAWeo130_assertion evidence source_evidence_curated NP177.RAI9vLIMKc1LoI8jOmSkVOAc1IxrtzWyulcjMpEjAAWeo130_provenance.
- NP177.RAI9vLIMKc1LoI8jOmSkVOAc1IxrtzWyulcjMpEjAAWeo130_assertion SIO_000772 19085907 NP177.RAI9vLIMKc1LoI8jOmSkVOAc1IxrtzWyulcjMpEjAAWeo130_provenance.
- NP177.RAI9vLIMKc1LoI8jOmSkVOAc1IxrtzWyulcjMpEjAAWeo130_assertion wasDerivedFrom uniprot-20130724 NP177.RAI9vLIMKc1LoI8jOmSkVOAc1IxrtzWyulcjMpEjAAWeo130_provenance.
- NP177.RAI9vLIMKc1LoI8jOmSkVOAc1IxrtzWyulcjMpEjAAWeo130_assertion wasGeneratedBy ECO_0000218 NP177.RAI9vLIMKc1LoI8jOmSkVOAc1IxrtzWyulcjMpEjAAWeo130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP177.RAI9vLIMKc1LoI8jOmSkVOAc1IxrtzWyulcjMpEjAAWeo130_provenance.