Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP959284.RA1h81FoOL65LsHM2Y5RB8KnxFZDZ6S_k39-lNGaEYz58130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP959284.RA1h81FoOL65LsHM2Y5RB8KnxFZDZ6S_k39-lNGaEYz58130_assertion type Assertion NP959284.RA1h81FoOL65LsHM2Y5RB8KnxFZDZ6S_k39-lNGaEYz58130_head.
- NP959284.RA1h81FoOL65LsHM2Y5RB8KnxFZDZ6S_k39-lNGaEYz58130_assertion description "[Deficiency of the paternal 15q11-q13 snoRNA HBII-85 locus is necessary to cause the neurodevelopmental disorder Prader-Willi syndrome (PWS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959284.RA1h81FoOL65LsHM2Y5RB8KnxFZDZ6S_k39-lNGaEYz58130_provenance.
- NP959284.RA1h81FoOL65LsHM2Y5RB8KnxFZDZ6S_k39-lNGaEYz58130_assertion evidence source_evidence_literature NP959284.RA1h81FoOL65LsHM2Y5RB8KnxFZDZ6S_k39-lNGaEYz58130_provenance.
- NP959284.RA1h81FoOL65LsHM2Y5RB8KnxFZDZ6S_k39-lNGaEYz58130_assertion SIO_000772 19656775 NP959284.RA1h81FoOL65LsHM2Y5RB8KnxFZDZ6S_k39-lNGaEYz58130_provenance.
- NP959284.RA1h81FoOL65LsHM2Y5RB8KnxFZDZ6S_k39-lNGaEYz58130_assertion wasDerivedFrom befree-20150227 NP959284.RA1h81FoOL65LsHM2Y5RB8KnxFZDZ6S_k39-lNGaEYz58130_provenance.
- NP959284.RA1h81FoOL65LsHM2Y5RB8KnxFZDZ6S_k39-lNGaEYz58130_assertion wasGeneratedBy ECO_0000203 NP959284.RA1h81FoOL65LsHM2Y5RB8KnxFZDZ6S_k39-lNGaEYz58130_provenance.