Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP786199.RAiZh5ivvv8OU8PGB1ihgcniFDTITcTj2-EMpNJjUYjVg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP786199.RAiZh5ivvv8OU8PGB1ihgcniFDTITcTj2-EMpNJjUYjVg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP786199.RAiZh5ivvv8OU8PGB1ihgcniFDTITcTj2-EMpNJjUYjVg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP786199.RAiZh5ivvv8OU8PGB1ihgcniFDTITcTj2-EMpNJjUYjVg130_provenance.
- NP786199.RAiZh5ivvv8OU8PGB1ihgcniFDTITcTj2-EMpNJjUYjVg130_assertion description "[XMESID is associated with a missense mutation in ARX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP786199.RAiZh5ivvv8OU8PGB1ihgcniFDTITcTj2-EMpNJjUYjVg130_provenance.
- NP786199.RAiZh5ivvv8OU8PGB1ihgcniFDTITcTj2-EMpNJjUYjVg130_assertion evidence source_evidence_literature NP786199.RAiZh5ivvv8OU8PGB1ihgcniFDTITcTj2-EMpNJjUYjVg130_provenance.
- NP786199.RAiZh5ivvv8OU8PGB1ihgcniFDTITcTj2-EMpNJjUYjVg130_assertion SIO_000772 12177367 NP786199.RAiZh5ivvv8OU8PGB1ihgcniFDTITcTj2-EMpNJjUYjVg130_provenance.
- NP786199.RAiZh5ivvv8OU8PGB1ihgcniFDTITcTj2-EMpNJjUYjVg130_assertion wasDerivedFrom befree-20140225 NP786199.RAiZh5ivvv8OU8PGB1ihgcniFDTITcTj2-EMpNJjUYjVg130_provenance.
- NP786199.RAiZh5ivvv8OU8PGB1ihgcniFDTITcTj2-EMpNJjUYjVg130_assertion wasGeneratedBy ECO_0000203 NP786199.RAiZh5ivvv8OU8PGB1ihgcniFDTITcTj2-EMpNJjUYjVg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP786199.RAiZh5ivvv8OU8PGB1ihgcniFDTITcTj2-EMpNJjUYjVg130_provenance.