Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP421370.RANMRnsFdpnZj5WAT5MLWgS7LctWBnHfl_mUW25H8ZfLQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP421370.RANMRnsFdpnZj5WAT5MLWgS7LctWBnHfl_mUW25H8ZfLQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP421370.RANMRnsFdpnZj5WAT5MLWgS7LctWBnHfl_mUW25H8ZfLQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP421370.RANMRnsFdpnZj5WAT5MLWgS7LctWBnHfl_mUW25H8ZfLQ130_provenance.
- NP421370.RANMRnsFdpnZj5WAT5MLWgS7LctWBnHfl_mUW25H8ZfLQ130_assertion description "[ARX mutation testing should be undertaken in children aged less than 1 year with Ohtahara syndrome and a movement disorder, and in infants with unexplained neurodegeneration, progressive white matter loss, and cortical atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP421370.RANMRnsFdpnZj5WAT5MLWgS7LctWBnHfl_mUW25H8ZfLQ130_provenance.
- NP421370.RANMRnsFdpnZj5WAT5MLWgS7LctWBnHfl_mUW25H8ZfLQ130_assertion evidence source_evidence_literature NP421370.RANMRnsFdpnZj5WAT5MLWgS7LctWBnHfl_mUW25H8ZfLQ130_provenance.
- NP421370.RANMRnsFdpnZj5WAT5MLWgS7LctWBnHfl_mUW25H8ZfLQ130_assertion SIO_000772 19747203 NP421370.RANMRnsFdpnZj5WAT5MLWgS7LctWBnHfl_mUW25H8ZfLQ130_provenance.
- NP421370.RANMRnsFdpnZj5WAT5MLWgS7LctWBnHfl_mUW25H8ZfLQ130_assertion wasDerivedFrom befree-20140225 NP421370.RANMRnsFdpnZj5WAT5MLWgS7LctWBnHfl_mUW25H8ZfLQ130_provenance.
- NP421370.RANMRnsFdpnZj5WAT5MLWgS7LctWBnHfl_mUW25H8ZfLQ130_assertion wasGeneratedBy ECO_0000203 NP421370.RANMRnsFdpnZj5WAT5MLWgS7LctWBnHfl_mUW25H8ZfLQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP421370.RANMRnsFdpnZj5WAT5MLWgS7LctWBnHfl_mUW25H8ZfLQ130_provenance.