Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP673737.RAf_fm_NlAKWSlQ2GfxYW41WrFhIUQy5Qi8Q8dPXMBnZw130_assertion> ?p ?o ?g. }
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- NP673737.RAf_fm_NlAKWSlQ2GfxYW41WrFhIUQy5Qi8Q8dPXMBnZw130_assertion type Assertion NP673737.RAf_fm_NlAKWSlQ2GfxYW41WrFhIUQy5Qi8Q8dPXMBnZw130_head.
- NP673737.RAf_fm_NlAKWSlQ2GfxYW41WrFhIUQy5Qi8Q8dPXMBnZw130_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." NP673737.RAf_fm_NlAKWSlQ2GfxYW41WrFhIUQy5Qi8Q8dPXMBnZw130_provenance.
- NP673737.RAf_fm_NlAKWSlQ2GfxYW41WrFhIUQy5Qi8Q8dPXMBnZw130_assertion evidence source_evidence_literature NP673737.RAf_fm_NlAKWSlQ2GfxYW41WrFhIUQy5Qi8Q8dPXMBnZw130_provenance.
- NP673737.RAf_fm_NlAKWSlQ2GfxYW41WrFhIUQy5Qi8Q8dPXMBnZw130_assertion SIO_000772 19656775 NP673737.RAf_fm_NlAKWSlQ2GfxYW41WrFhIUQy5Qi8Q8dPXMBnZw130_provenance.
- NP673737.RAf_fm_NlAKWSlQ2GfxYW41WrFhIUQy5Qi8Q8dPXMBnZw130_assertion wasDerivedFrom befree-20150227 NP673737.RAf_fm_NlAKWSlQ2GfxYW41WrFhIUQy5Qi8Q8dPXMBnZw130_provenance.
- NP673737.RAf_fm_NlAKWSlQ2GfxYW41WrFhIUQy5Qi8Q8dPXMBnZw130_assertion wasGeneratedBy ECO_0000203 NP673737.RAf_fm_NlAKWSlQ2GfxYW41WrFhIUQy5Qi8Q8dPXMBnZw130_provenance.