Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP521251.RAlgjwwX3msifcjkNRg1KfbIWx72LmCIzglTrzznufPAQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP521251.RAlgjwwX3msifcjkNRg1KfbIWx72LmCIzglTrzznufPAQ130_assertion type Assertion NP521251.RAlgjwwX3msifcjkNRg1KfbIWx72LmCIzglTrzznufPAQ130_head.
- NP521251.RAlgjwwX3msifcjkNRg1KfbIWx72LmCIzglTrzznufPAQ130_assertion description "[Comparison of the phenotypic features in a total of 19 patients with del(17)(p11.2p11.2) shows a consistent clinical phenotype with moderate to severe mental retardation, microbrachycelphaly, prominent forehead, broad face, flat midface, prognathism, short, broad hands, and behavioural anomalies such as self-mutilation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521251.RAlgjwwX3msifcjkNRg1KfbIWx72LmCIzglTrzznufPAQ130_provenance.
- NP521251.RAlgjwwX3msifcjkNRg1KfbIWx72LmCIzglTrzznufPAQ130_assertion evidence source_evidence_literature NP521251.RAlgjwwX3msifcjkNRg1KfbIWx72LmCIzglTrzznufPAQ130_provenance.
- NP521251.RAlgjwwX3msifcjkNRg1KfbIWx72LmCIzglTrzznufPAQ130_assertion SIO_000772 3236351 NP521251.RAlgjwwX3msifcjkNRg1KfbIWx72LmCIzglTrzznufPAQ130_provenance.
- NP521251.RAlgjwwX3msifcjkNRg1KfbIWx72LmCIzglTrzznufPAQ130_assertion wasDerivedFrom befree-20140225 NP521251.RAlgjwwX3msifcjkNRg1KfbIWx72LmCIzglTrzznufPAQ130_provenance.
- NP521251.RAlgjwwX3msifcjkNRg1KfbIWx72LmCIzglTrzznufPAQ130_assertion wasGeneratedBy ECO_0000203 NP521251.RAlgjwwX3msifcjkNRg1KfbIWx72LmCIzglTrzznufPAQ130_provenance.