Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP433170.RAWn1c-MpnJXiJon80Hyi1N2vCT_8z8PawaNE6gUkhAas130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP433170.RAWn1c-MpnJXiJon80Hyi1N2vCT_8z8PawaNE6gUkhAas130_assertion type Assertion NP433170.RAWn1c-MpnJXiJon80Hyi1N2vCT_8z8PawaNE6gUkhAas130_head.
- NP433170.RAWn1c-MpnJXiJon80Hyi1N2vCT_8z8PawaNE6gUkhAas130_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." NP433170.RAWn1c-MpnJXiJon80Hyi1N2vCT_8z8PawaNE6gUkhAas130_provenance.
- NP433170.RAWn1c-MpnJXiJon80Hyi1N2vCT_8z8PawaNE6gUkhAas130_assertion evidence source_evidence_literature NP433170.RAWn1c-MpnJXiJon80Hyi1N2vCT_8z8PawaNE6gUkhAas130_provenance.
- NP433170.RAWn1c-MpnJXiJon80Hyi1N2vCT_8z8PawaNE6gUkhAas130_assertion SIO_000772 19656775 NP433170.RAWn1c-MpnJXiJon80Hyi1N2vCT_8z8PawaNE6gUkhAas130_provenance.
- NP433170.RAWn1c-MpnJXiJon80Hyi1N2vCT_8z8PawaNE6gUkhAas130_assertion wasDerivedFrom befree-20140225 NP433170.RAWn1c-MpnJXiJon80Hyi1N2vCT_8z8PawaNE6gUkhAas130_provenance.
- NP433170.RAWn1c-MpnJXiJon80Hyi1N2vCT_8z8PawaNE6gUkhAas130_assertion wasGeneratedBy ECO_0000203 NP433170.RAWn1c-MpnJXiJon80Hyi1N2vCT_8z8PawaNE6gUkhAas130_provenance.