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- source_evidence_literature type ECO_0000212 NP978113.RAzx0T-yhPQhgbl-XAtEsDmUGj2g3L7oFTxeuxfc7-qVg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978113.RAzx0T-yhPQhgbl-XAtEsDmUGj2g3L7oFTxeuxfc7-qVg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978113.RAzx0T-yhPQhgbl-XAtEsDmUGj2g3L7oFTxeuxfc7-qVg130_provenance.
- NP978113.RAzx0T-yhPQhgbl-XAtEsDmUGj2g3L7oFTxeuxfc7-qVg130_assertion description "[Aristaless-related homeobox gene (ARX) mutation leads to several neurological disorders including X-linked lissencephaly with abnormal genitalia (XLAG), West syndrome and Partington syndrome, with XLAG being the most severe form.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978113.RAzx0T-yhPQhgbl-XAtEsDmUGj2g3L7oFTxeuxfc7-qVg130_provenance.
- NP978113.RAzx0T-yhPQhgbl-XAtEsDmUGj2g3L7oFTxeuxfc7-qVg130_assertion evidence source_evidence_literature NP978113.RAzx0T-yhPQhgbl-XAtEsDmUGj2g3L7oFTxeuxfc7-qVg130_provenance.
- NP978113.RAzx0T-yhPQhgbl-XAtEsDmUGj2g3L7oFTxeuxfc7-qVg130_assertion SIO_000772 20538404 NP978113.RAzx0T-yhPQhgbl-XAtEsDmUGj2g3L7oFTxeuxfc7-qVg130_provenance.
- NP978113.RAzx0T-yhPQhgbl-XAtEsDmUGj2g3L7oFTxeuxfc7-qVg130_assertion wasDerivedFrom befree-20150227 NP978113.RAzx0T-yhPQhgbl-XAtEsDmUGj2g3L7oFTxeuxfc7-qVg130_provenance.
- NP978113.RAzx0T-yhPQhgbl-XAtEsDmUGj2g3L7oFTxeuxfc7-qVg130_assertion wasGeneratedBy ECO_0000203 NP978113.RAzx0T-yhPQhgbl-XAtEsDmUGj2g3L7oFTxeuxfc7-qVg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978113.RAzx0T-yhPQhgbl-XAtEsDmUGj2g3L7oFTxeuxfc7-qVg130_provenance.