Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP782722.RAsmPJIiEgd32qoOcQwULDuo6Sk6A4QDt5UvVcG19sFsw130_assertion> ?p ?o ?g. }
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- NP782722.RAsmPJIiEgd32qoOcQwULDuo6Sk6A4QDt5UvVcG19sFsw130_assertion type Assertion NP782722.RAsmPJIiEgd32qoOcQwULDuo6Sk6A4QDt5UvVcG19sFsw130_head.
- NP782722.RAsmPJIiEgd32qoOcQwULDuo6Sk6A4QDt5UvVcG19sFsw130_assertion description "[Therefore, ZNF127 and ZNF127AS are novel imprinted genes that may be associated with some of the clinical features of the polygenic Prader-Willi syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782722.RAsmPJIiEgd32qoOcQwULDuo6Sk6A4QDt5UvVcG19sFsw130_provenance.
- NP782722.RAsmPJIiEgd32qoOcQwULDuo6Sk6A4QDt5UvVcG19sFsw130_assertion evidence source_evidence_literature NP782722.RAsmPJIiEgd32qoOcQwULDuo6Sk6A4QDt5UvVcG19sFsw130_provenance.
- NP782722.RAsmPJIiEgd32qoOcQwULDuo6Sk6A4QDt5UvVcG19sFsw130_assertion SIO_000772 10196367 NP782722.RAsmPJIiEgd32qoOcQwULDuo6Sk6A4QDt5UvVcG19sFsw130_provenance.
- NP782722.RAsmPJIiEgd32qoOcQwULDuo6Sk6A4QDt5UvVcG19sFsw130_assertion wasDerivedFrom befree-20150227 NP782722.RAsmPJIiEgd32qoOcQwULDuo6Sk6A4QDt5UvVcG19sFsw130_provenance.
- NP782722.RAsmPJIiEgd32qoOcQwULDuo6Sk6A4QDt5UvVcG19sFsw130_assertion wasGeneratedBy ECO_0000203 NP782722.RAsmPJIiEgd32qoOcQwULDuo6Sk6A4QDt5UvVcG19sFsw130_provenance.