Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP4930.RAgHBhah_wNYyDV8WepM4vMjHk6MDQ3VrXT4D51QqrzME130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4930.RAgHBhah_wNYyDV8WepM4vMjHk6MDQ3VrXT4D51QqrzME130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4930.RAgHBhah_wNYyDV8WepM4vMjHk6MDQ3VrXT4D51QqrzME130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4930.RAgHBhah_wNYyDV8WepM4vMjHk6MDQ3VrXT4D51QqrzME130_provenance.
- NP4930.RAgHBhah_wNYyDV8WepM4vMjHk6MDQ3VrXT4D51QqrzME130_assertion description "[An osteopenic nonfracture syndrome with features of mild osteogenesis imperfecta associated with the substitution of a cysteine for glycine at triple helix position 43 in the pro alpha 1(I) chain of type I collagen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4930.RAgHBhah_wNYyDV8WepM4vMjHk6MDQ3VrXT4D51QqrzME130_provenance.
- NP4930.RAgHBhah_wNYyDV8WepM4vMjHk6MDQ3VrXT4D51QqrzME130_assertion evidence source_evidence_curated NP4930.RAgHBhah_wNYyDV8WepM4vMjHk6MDQ3VrXT4D51QqrzME130_provenance.
- NP4930.RAgHBhah_wNYyDV8WepM4vMjHk6MDQ3VrXT4D51QqrzME130_assertion SIO_000772 1737847 NP4930.RAgHBhah_wNYyDV8WepM4vMjHk6MDQ3VrXT4D51QqrzME130_provenance.
- NP4930.RAgHBhah_wNYyDV8WepM4vMjHk6MDQ3VrXT4D51QqrzME130_assertion wasDerivedFrom uniprot-2016 NP4930.RAgHBhah_wNYyDV8WepM4vMjHk6MDQ3VrXT4D51QqrzME130_provenance.
- NP4930.RAgHBhah_wNYyDV8WepM4vMjHk6MDQ3VrXT4D51QqrzME130_assertion wasGeneratedBy ECO_0000218 NP4930.RAgHBhah_wNYyDV8WepM4vMjHk6MDQ3VrXT4D51QqrzME130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP4930.RAgHBhah_wNYyDV8WepM4vMjHk6MDQ3VrXT4D51QqrzME130_provenance.