Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP279677.RAMBPkTxNFktT1RlgUPnRU_upHSehNqz2NpHw27jjbM14130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP279677.RAMBPkTxNFktT1RlgUPnRU_upHSehNqz2NpHw27jjbM14130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP279677.RAMBPkTxNFktT1RlgUPnRU_upHSehNqz2NpHw27jjbM14130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP279677.RAMBPkTxNFktT1RlgUPnRU_upHSehNqz2NpHw27jjbM14130_provenance.
- NP279677.RAMBPkTxNFktT1RlgUPnRU_upHSehNqz2NpHw27jjbM14130_assertion description "[Recently, longer expansion of the first polyalanine tract of ARX was found to be causative for Ohtahara syndrome without brain malformation, whereas premature termination mutations of ARX were found to cause severe brain malformations, such as lissencephaly or hydranencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279677.RAMBPkTxNFktT1RlgUPnRU_upHSehNqz2NpHw27jjbM14130_provenance.
- NP279677.RAMBPkTxNFktT1RlgUPnRU_upHSehNqz2NpHw27jjbM14130_assertion evidence source_evidence_literature NP279677.RAMBPkTxNFktT1RlgUPnRU_upHSehNqz2NpHw27jjbM14130_provenance.
- NP279677.RAMBPkTxNFktT1RlgUPnRU_upHSehNqz2NpHw27jjbM14130_assertion SIO_000772 20384723 NP279677.RAMBPkTxNFktT1RlgUPnRU_upHSehNqz2NpHw27jjbM14130_provenance.
- NP279677.RAMBPkTxNFktT1RlgUPnRU_upHSehNqz2NpHw27jjbM14130_assertion wasDerivedFrom befree-20140225 NP279677.RAMBPkTxNFktT1RlgUPnRU_upHSehNqz2NpHw27jjbM14130_provenance.
- NP279677.RAMBPkTxNFktT1RlgUPnRU_upHSehNqz2NpHw27jjbM14130_assertion wasGeneratedBy ECO_0000203 NP279677.RAMBPkTxNFktT1RlgUPnRU_upHSehNqz2NpHw27jjbM14130_provenance.
- befree-20140225 importedOn "2014-02-25" NP279677.RAMBPkTxNFktT1RlgUPnRU_upHSehNqz2NpHw27jjbM14130_provenance.