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- source_evidence_literature type ECO_0000212 NP921814.RAbt3M4MR4csvKanMW6pTYQtcsVFzaIco0Lmq-Uu__Rew130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP921814.RAbt3M4MR4csvKanMW6pTYQtcsVFzaIco0Lmq-Uu__Rew130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP921814.RAbt3M4MR4csvKanMW6pTYQtcsVFzaIco0Lmq-Uu__Rew130_provenance.
- NP921814.RAbt3M4MR4csvKanMW6pTYQtcsVFzaIco0Lmq-Uu__Rew130_assertion description "[Detection of classical 17p11.2 deletions, an atypical deletion and RAI1 alterations in patients with features suggestive of Smith-Magenis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921814.RAbt3M4MR4csvKanMW6pTYQtcsVFzaIco0Lmq-Uu__Rew130_provenance.
- NP921814.RAbt3M4MR4csvKanMW6pTYQtcsVFzaIco0Lmq-Uu__Rew130_assertion evidence source_evidence_literature NP921814.RAbt3M4MR4csvKanMW6pTYQtcsVFzaIco0Lmq-Uu__Rew130_provenance.
- NP921814.RAbt3M4MR4csvKanMW6pTYQtcsVFzaIco0Lmq-Uu__Rew130_assertion SIO_000772 21897445 NP921814.RAbt3M4MR4csvKanMW6pTYQtcsVFzaIco0Lmq-Uu__Rew130_provenance.
- NP921814.RAbt3M4MR4csvKanMW6pTYQtcsVFzaIco0Lmq-Uu__Rew130_assertion wasDerivedFrom befree-2016 NP921814.RAbt3M4MR4csvKanMW6pTYQtcsVFzaIco0Lmq-Uu__Rew130_provenance.
- NP921814.RAbt3M4MR4csvKanMW6pTYQtcsVFzaIco0Lmq-Uu__Rew130_assertion wasGeneratedBy ECO_0000203 NP921814.RAbt3M4MR4csvKanMW6pTYQtcsVFzaIco0Lmq-Uu__Rew130_provenance.
- befree-2016 importedOn "2016-02-19" NP921814.RAbt3M4MR4csvKanMW6pTYQtcsVFzaIco0Lmq-Uu__Rew130_provenance.