Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6333.RA2BfYMPoCyrQOw8VjH4wHg8CI1ccLVKVFrRFZ6sL4QNE130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6333.RA2BfYMPoCyrQOw8VjH4wHg8CI1ccLVKVFrRFZ6sL4QNE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6333.RA2BfYMPoCyrQOw8VjH4wHg8CI1ccLVKVFrRFZ6sL4QNE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6333.RA2BfYMPoCyrQOw8VjH4wHg8CI1ccLVKVFrRFZ6sL4QNE130_provenance.
- NP6333.RA2BfYMPoCyrQOw8VjH4wHg8CI1ccLVKVFrRFZ6sL4QNE130_assertion description "[De novo ACTA2 mutation causes a novel syndrome of multisystemic smooth muscle dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6333.RA2BfYMPoCyrQOw8VjH4wHg8CI1ccLVKVFrRFZ6sL4QNE130_provenance.
- NP6333.RA2BfYMPoCyrQOw8VjH4wHg8CI1ccLVKVFrRFZ6sL4QNE130_assertion evidence source_evidence_curated NP6333.RA2BfYMPoCyrQOw8VjH4wHg8CI1ccLVKVFrRFZ6sL4QNE130_provenance.
- NP6333.RA2BfYMPoCyrQOw8VjH4wHg8CI1ccLVKVFrRFZ6sL4QNE130_assertion SIO_000772 20734336 NP6333.RA2BfYMPoCyrQOw8VjH4wHg8CI1ccLVKVFrRFZ6sL4QNE130_provenance.
- NP6333.RA2BfYMPoCyrQOw8VjH4wHg8CI1ccLVKVFrRFZ6sL4QNE130_assertion wasDerivedFrom uniprot-2016 NP6333.RA2BfYMPoCyrQOw8VjH4wHg8CI1ccLVKVFrRFZ6sL4QNE130_provenance.
- NP6333.RA2BfYMPoCyrQOw8VjH4wHg8CI1ccLVKVFrRFZ6sL4QNE130_assertion wasGeneratedBy ECO_0000218 NP6333.RA2BfYMPoCyrQOw8VjH4wHg8CI1ccLVKVFrRFZ6sL4QNE130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6333.RA2BfYMPoCyrQOw8VjH4wHg8CI1ccLVKVFrRFZ6sL4QNE130_provenance.