Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP669580.RAO7l6sNSLy_q5PWdcawjBRNpxk4o-oMUT6pZpCweWaYE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP669580.RAO7l6sNSLy_q5PWdcawjBRNpxk4o-oMUT6pZpCweWaYE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP669580.RAO7l6sNSLy_q5PWdcawjBRNpxk4o-oMUT6pZpCweWaYE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP669580.RAO7l6sNSLy_q5PWdcawjBRNpxk4o-oMUT6pZpCweWaYE130_provenance.
- NP669580.RAO7l6sNSLy_q5PWdcawjBRNpxk4o-oMUT6pZpCweWaYE130_assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP669580.RAO7l6sNSLy_q5PWdcawjBRNpxk4o-oMUT6pZpCweWaYE130_provenance.
- NP669580.RAO7l6sNSLy_q5PWdcawjBRNpxk4o-oMUT6pZpCweWaYE130_assertion evidence source_evidence_literature NP669580.RAO7l6sNSLy_q5PWdcawjBRNpxk4o-oMUT6pZpCweWaYE130_provenance.
- NP669580.RAO7l6sNSLy_q5PWdcawjBRNpxk4o-oMUT6pZpCweWaYE130_assertion SIO_000772 10982188 NP669580.RAO7l6sNSLy_q5PWdcawjBRNpxk4o-oMUT6pZpCweWaYE130_provenance.
- NP669580.RAO7l6sNSLy_q5PWdcawjBRNpxk4o-oMUT6pZpCweWaYE130_assertion wasDerivedFrom befree-20140225 NP669580.RAO7l6sNSLy_q5PWdcawjBRNpxk4o-oMUT6pZpCweWaYE130_provenance.
- NP669580.RAO7l6sNSLy_q5PWdcawjBRNpxk4o-oMUT6pZpCweWaYE130_assertion wasGeneratedBy ECO_0000203 NP669580.RAO7l6sNSLy_q5PWdcawjBRNpxk4o-oMUT6pZpCweWaYE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP669580.RAO7l6sNSLy_q5PWdcawjBRNpxk4o-oMUT6pZpCweWaYE130_provenance.