Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP183479.RA42z6A3smzk9oaQReyS_sYcyiLRFhma95oDsw_bK6kfg130_assertion> ?p ?o ?g. }
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- NP183479.RA42z6A3smzk9oaQReyS_sYcyiLRFhma95oDsw_bK6kfg130_assertion type Assertion NP183479.RA42z6A3smzk9oaQReyS_sYcyiLRFhma95oDsw_bK6kfg130_head.
- NP183479.RA42z6A3smzk9oaQReyS_sYcyiLRFhma95oDsw_bK6kfg130_assertion description "[a possibly inactivating mutation in the SNRPN minimal promoter region was identified in Prader-Willi syndrome]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183479.RA42z6A3smzk9oaQReyS_sYcyiLRFhma95oDsw_bK6kfg130_provenance.
- NP183479.RA42z6A3smzk9oaQReyS_sYcyiLRFhma95oDsw_bK6kfg130_assertion evidence source_evidence_literature NP183479.RA42z6A3smzk9oaQReyS_sYcyiLRFhma95oDsw_bK6kfg130_provenance.
- NP183479.RA42z6A3smzk9oaQReyS_sYcyiLRFhma95oDsw_bK6kfg130_assertion SIO_000772 17262171 NP183479.RA42z6A3smzk9oaQReyS_sYcyiLRFhma95oDsw_bK6kfg130_provenance.
- NP183479.RA42z6A3smzk9oaQReyS_sYcyiLRFhma95oDsw_bK6kfg130_assertion wasDerivedFrom lhgdn-20090331 NP183479.RA42z6A3smzk9oaQReyS_sYcyiLRFhma95oDsw_bK6kfg130_provenance.
- NP183479.RA42z6A3smzk9oaQReyS_sYcyiLRFhma95oDsw_bK6kfg130_assertion wasGeneratedBy ECO_0000203 NP183479.RA42z6A3smzk9oaQReyS_sYcyiLRFhma95oDsw_bK6kfg130_provenance.