Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP5749.RArxQIGgrHnBfoQsbCCtRNGJJ31XAuxXGhUl_m7oKtja4130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP5749.RArxQIGgrHnBfoQsbCCtRNGJJ31XAuxXGhUl_m7oKtja4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5749.RArxQIGgrHnBfoQsbCCtRNGJJ31XAuxXGhUl_m7oKtja4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5749.RArxQIGgrHnBfoQsbCCtRNGJJ31XAuxXGhUl_m7oKtja4130_provenance.
- NP5749.RArxQIGgrHnBfoQsbCCtRNGJJ31XAuxXGhUl_m7oKtja4130_assertion description "[Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5749.RArxQIGgrHnBfoQsbCCtRNGJJ31XAuxXGhUl_m7oKtja4130_provenance.
- NP5749.RArxQIGgrHnBfoQsbCCtRNGJJ31XAuxXGhUl_m7oKtja4130_assertion evidence source_evidence_curated NP5749.RArxQIGgrHnBfoQsbCCtRNGJJ31XAuxXGhUl_m7oKtja4130_provenance.
- NP5749.RArxQIGgrHnBfoQsbCCtRNGJJ31XAuxXGhUl_m7oKtja4130_assertion SIO_000772 19330033 NP5749.RArxQIGgrHnBfoQsbCCtRNGJJ31XAuxXGhUl_m7oKtja4130_provenance.
- NP5749.RArxQIGgrHnBfoQsbCCtRNGJJ31XAuxXGhUl_m7oKtja4130_assertion wasDerivedFrom uniprot-2016 NP5749.RArxQIGgrHnBfoQsbCCtRNGJJ31XAuxXGhUl_m7oKtja4130_provenance.
- NP5749.RArxQIGgrHnBfoQsbCCtRNGJJ31XAuxXGhUl_m7oKtja4130_assertion wasGeneratedBy ECO_0000218 NP5749.RArxQIGgrHnBfoQsbCCtRNGJJ31XAuxXGhUl_m7oKtja4130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP5749.RArxQIGgrHnBfoQsbCCtRNGJJ31XAuxXGhUl_m7oKtja4130_provenance.