Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP310201.RAbbgYbLvOq_Mqd8zje84KXy7MqkjduApfGZPvkfZP8ng130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP310201.RAbbgYbLvOq_Mqd8zje84KXy7MqkjduApfGZPvkfZP8ng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP310201.RAbbgYbLvOq_Mqd8zje84KXy7MqkjduApfGZPvkfZP8ng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP310201.RAbbgYbLvOq_Mqd8zje84KXy7MqkjduApfGZPvkfZP8ng130_provenance.
- NP310201.RAbbgYbLvOq_Mqd8zje84KXy7MqkjduApfGZPvkfZP8ng130_assertion description "[Mutations in the human ARX gene have been shown to cause nonsyndromic X-linked mental retardation (MRX) as well as syndromic forms such as X-linked lissencephaly with abnormal genitalia (XLAG), Partington syndrome and X-linked infantile spasm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP310201.RAbbgYbLvOq_Mqd8zje84KXy7MqkjduApfGZPvkfZP8ng130_provenance.
- NP310201.RAbbgYbLvOq_Mqd8zje84KXy7MqkjduApfGZPvkfZP8ng130_assertion evidence source_evidence_literature NP310201.RAbbgYbLvOq_Mqd8zje84KXy7MqkjduApfGZPvkfZP8ng130_provenance.
- NP310201.RAbbgYbLvOq_Mqd8zje84KXy7MqkjduApfGZPvkfZP8ng130_assertion SIO_000772 16235064 NP310201.RAbbgYbLvOq_Mqd8zje84KXy7MqkjduApfGZPvkfZP8ng130_provenance.
- NP310201.RAbbgYbLvOq_Mqd8zje84KXy7MqkjduApfGZPvkfZP8ng130_assertion wasDerivedFrom befree-20140225 NP310201.RAbbgYbLvOq_Mqd8zje84KXy7MqkjduApfGZPvkfZP8ng130_provenance.
- NP310201.RAbbgYbLvOq_Mqd8zje84KXy7MqkjduApfGZPvkfZP8ng130_assertion wasGeneratedBy ECO_0000203 NP310201.RAbbgYbLvOq_Mqd8zje84KXy7MqkjduApfGZPvkfZP8ng130_provenance.
- befree-20140225 importedOn "2014-02-25" NP310201.RAbbgYbLvOq_Mqd8zje84KXy7MqkjduApfGZPvkfZP8ng130_provenance.