Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP203698.RACFXYYu7PBAclXEZln3_CM8ZNTgnJLfXBk_nY5nUEdq4130_assertion> ?p ?o ?g. }
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- NP203698.RACFXYYu7PBAclXEZln3_CM8ZNTgnJLfXBk_nY5nUEdq4130_assertion type Assertion NP203698.RACFXYYu7PBAclXEZln3_CM8ZNTgnJLfXBk_nY5nUEdq4130_head.
- NP203698.RACFXYYu7PBAclXEZln3_CM8ZNTgnJLfXBk_nY5nUEdq4130_assertion wasGeneratedBy ECO_0000203 NP203698.RACFXYYu7PBAclXEZln3_CM8ZNTgnJLfXBk_nY5nUEdq4130_provenance.
- NP203698.RACFXYYu7PBAclXEZln3_CM8ZNTgnJLfXBk_nY5nUEdq4130_assertion wasDerivedFrom lhgdn-20090331 NP203698.RACFXYYu7PBAclXEZln3_CM8ZNTgnJLfXBk_nY5nUEdq4130_provenance.
- NP203698.RACFXYYu7PBAclXEZln3_CM8ZNTgnJLfXBk_nY5nUEdq4130_assertion SIO_000772 14981720 NP203698.RACFXYYu7PBAclXEZln3_CM8ZNTgnJLfXBk_nY5nUEdq4130_provenance.
- NP203698.RACFXYYu7PBAclXEZln3_CM8ZNTgnJLfXBk_nY5nUEdq4130_assertion evidence source_evidence_literature NP203698.RACFXYYu7PBAclXEZln3_CM8ZNTgnJLfXBk_nY5nUEdq4130_provenance.
- NP203698.RACFXYYu7PBAclXEZln3_CM8ZNTgnJLfXBk_nY5nUEdq4130_assertion description "[A daughter who carried the der Y had the clinical features of Prader-Willi syndrome while a son who carries the der 15 has mild developmental delay and hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP203698.RACFXYYu7PBAclXEZln3_CM8ZNTgnJLfXBk_nY5nUEdq4130_provenance.