Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP187389.RA0jaRNPh30wwi43xZRveHY0ZwIq6v574NmWf4GfXk6gA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP187389.RA0jaRNPh30wwi43xZRveHY0ZwIq6v574NmWf4GfXk6gA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP187389.RA0jaRNPh30wwi43xZRveHY0ZwIq6v574NmWf4GfXk6gA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP187389.RA0jaRNPh30wwi43xZRveHY0ZwIq6v574NmWf4GfXk6gA130_provenance.
- NP187389.RA0jaRNPh30wwi43xZRveHY0ZwIq6v574NmWf4GfXk6gA130_assertion description "[This study reports a novel 24-bp in-frame deletion within exon 2 of the ARX gene in a male child with X-linked mental retardation]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187389.RA0jaRNPh30wwi43xZRveHY0ZwIq6v574NmWf4GfXk6gA130_provenance.
- NP187389.RA0jaRNPh30wwi43xZRveHY0ZwIq6v574NmWf4GfXk6gA130_assertion evidence source_evidence_literature NP187389.RA0jaRNPh30wwi43xZRveHY0ZwIq6v574NmWf4GfXk6gA130_provenance.
- NP187389.RA0jaRNPh30wwi43xZRveHY0ZwIq6v574NmWf4GfXk6gA130_assertion SIO_000772 17641262 NP187389.RA0jaRNPh30wwi43xZRveHY0ZwIq6v574NmWf4GfXk6gA130_provenance.
- NP187389.RA0jaRNPh30wwi43xZRveHY0ZwIq6v574NmWf4GfXk6gA130_assertion wasDerivedFrom lhgdn-20090331 NP187389.RA0jaRNPh30wwi43xZRveHY0ZwIq6v574NmWf4GfXk6gA130_provenance.
- NP187389.RA0jaRNPh30wwi43xZRveHY0ZwIq6v574NmWf4GfXk6gA130_assertion wasGeneratedBy ECO_0000203 NP187389.RA0jaRNPh30wwi43xZRveHY0ZwIq6v574NmWf4GfXk6gA130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP187389.RA0jaRNPh30wwi43xZRveHY0ZwIq6v574NmWf4GfXk6gA130_provenance.