Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP120289.RATdvM7qHRL0MuOU-SuD7omJdLkBYrPreSlnfbSz1CeCY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP120289.RATdvM7qHRL0MuOU-SuD7omJdLkBYrPreSlnfbSz1CeCY130_assertion type Assertion NP120289.RATdvM7qHRL0MuOU-SuD7omJdLkBYrPreSlnfbSz1CeCY130_head.
- NP120289.RATdvM7qHRL0MuOU-SuD7omJdLkBYrPreSlnfbSz1CeCY130_assertion wasGeneratedBy ECO_0000203 NP120289.RATdvM7qHRL0MuOU-SuD7omJdLkBYrPreSlnfbSz1CeCY130_provenance.
- NP120289.RATdvM7qHRL0MuOU-SuD7omJdLkBYrPreSlnfbSz1CeCY130_assertion wasDerivedFrom lhgdn-20090331 NP120289.RATdvM7qHRL0MuOU-SuD7omJdLkBYrPreSlnfbSz1CeCY130_provenance.
- NP120289.RATdvM7qHRL0MuOU-SuD7omJdLkBYrPreSlnfbSz1CeCY130_assertion SIO_000772 14981720 NP120289.RATdvM7qHRL0MuOU-SuD7omJdLkBYrPreSlnfbSz1CeCY130_provenance.
- NP120289.RATdvM7qHRL0MuOU-SuD7omJdLkBYrPreSlnfbSz1CeCY130_assertion evidence source_evidence_literature NP120289.RATdvM7qHRL0MuOU-SuD7omJdLkBYrPreSlnfbSz1CeCY130_provenance.
- NP120289.RATdvM7qHRL0MuOU-SuD7omJdLkBYrPreSlnfbSz1CeCY130_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." NP120289.RATdvM7qHRL0MuOU-SuD7omJdLkBYrPreSlnfbSz1CeCY130_provenance.