Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP787059.RAEYcSTcMrxbmL_FPU5H4qsppxSKiaS6sDfwlT6SOmA-s130_assertion> ?p ?o ?g. }
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- NP787059.RAEYcSTcMrxbmL_FPU5H4qsppxSKiaS6sDfwlT6SOmA-s130_assertion type Assertion NP787059.RAEYcSTcMrxbmL_FPU5H4qsppxSKiaS6sDfwlT6SOmA-s130_head.
- NP787059.RAEYcSTcMrxbmL_FPU5H4qsppxSKiaS6sDfwlT6SOmA-s130_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." NP787059.RAEYcSTcMrxbmL_FPU5H4qsppxSKiaS6sDfwlT6SOmA-s130_provenance.
- NP787059.RAEYcSTcMrxbmL_FPU5H4qsppxSKiaS6sDfwlT6SOmA-s130_assertion evidence source_evidence_literature NP787059.RAEYcSTcMrxbmL_FPU5H4qsppxSKiaS6sDfwlT6SOmA-s130_provenance.
- NP787059.RAEYcSTcMrxbmL_FPU5H4qsppxSKiaS6sDfwlT6SOmA-s130_assertion SIO_000772 20074076 NP787059.RAEYcSTcMrxbmL_FPU5H4qsppxSKiaS6sDfwlT6SOmA-s130_provenance.
- NP787059.RAEYcSTcMrxbmL_FPU5H4qsppxSKiaS6sDfwlT6SOmA-s130_assertion wasDerivedFrom befree-2016 NP787059.RAEYcSTcMrxbmL_FPU5H4qsppxSKiaS6sDfwlT6SOmA-s130_provenance.
- NP787059.RAEYcSTcMrxbmL_FPU5H4qsppxSKiaS6sDfwlT6SOmA-s130_assertion wasGeneratedBy ECO_0000203 NP787059.RAEYcSTcMrxbmL_FPU5H4qsppxSKiaS6sDfwlT6SOmA-s130_provenance.