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- source_evidence_literature type ECO_0000212 NP782722.RAsmPJIiEgd32qoOcQwULDuo6Sk6A4QDt5UvVcG19sFsw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP782722.RAsmPJIiEgd32qoOcQwULDuo6Sk6A4QDt5UvVcG19sFsw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP782722.RAsmPJIiEgd32qoOcQwULDuo6Sk6A4QDt5UvVcG19sFsw130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP782722.RAsmPJIiEgd32qoOcQwULDuo6Sk6A4QDt5UvVcG19sFsw130_provenance.