Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP787061.RA3j786jT36NPLMFRgjhQqYQFeb9TiPF07wD23SrtetsE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP787061.RA3j786jT36NPLMFRgjhQqYQFeb9TiPF07wD23SrtetsE130_assertion type Assertion NP787061.RA3j786jT36NPLMFRgjhQqYQFeb9TiPF07wD23SrtetsE130_head.
- NP787061.RA3j786jT36NPLMFRgjhQqYQFeb9TiPF07wD23SrtetsE130_assertion description "[HGPS (Hutchinson-Gilford progeria syndrome) is a rare genetic disease affecting children causing them to age and die prematurely.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787061.RA3j786jT36NPLMFRgjhQqYQFeb9TiPF07wD23SrtetsE130_provenance.
- NP787061.RA3j786jT36NPLMFRgjhQqYQFeb9TiPF07wD23SrtetsE130_assertion evidence source_evidence_literature NP787061.RA3j786jT36NPLMFRgjhQqYQFeb9TiPF07wD23SrtetsE130_provenance.
- NP787061.RA3j786jT36NPLMFRgjhQqYQFeb9TiPF07wD23SrtetsE130_assertion SIO_000772 20074076 NP787061.RA3j786jT36NPLMFRgjhQqYQFeb9TiPF07wD23SrtetsE130_provenance.
- NP787061.RA3j786jT36NPLMFRgjhQqYQFeb9TiPF07wD23SrtetsE130_assertion wasDerivedFrom befree-2016 NP787061.RA3j786jT36NPLMFRgjhQqYQFeb9TiPF07wD23SrtetsE130_provenance.
- NP787061.RA3j786jT36NPLMFRgjhQqYQFeb9TiPF07wD23SrtetsE130_assertion wasGeneratedBy ECO_0000203 NP787061.RA3j786jT36NPLMFRgjhQqYQFeb9TiPF07wD23SrtetsE130_provenance.