Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP470683.RA0d9og_cAcbvrp17L8kC9sDZnHRldGgR1ppZFakJVqPE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP470683.RA0d9og_cAcbvrp17L8kC9sDZnHRldGgR1ppZFakJVqPE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470683.RA0d9og_cAcbvrp17L8kC9sDZnHRldGgR1ppZFakJVqPE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470683.RA0d9og_cAcbvrp17L8kC9sDZnHRldGgR1ppZFakJVqPE130_provenance.
- NP470683.RA0d9og_cAcbvrp17L8kC9sDZnHRldGgR1ppZFakJVqPE130_assertion description "[Clinical utility of array CGH for the detection of chromosomal imbalances associated with mental retardation and multiple congenital anomalies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470683.RA0d9og_cAcbvrp17L8kC9sDZnHRldGgR1ppZFakJVqPE130_provenance.
- NP470683.RA0d9og_cAcbvrp17L8kC9sDZnHRldGgR1ppZFakJVqPE130_assertion evidence source_evidence_literature NP470683.RA0d9og_cAcbvrp17L8kC9sDZnHRldGgR1ppZFakJVqPE130_provenance.
- NP470683.RA0d9og_cAcbvrp17L8kC9sDZnHRldGgR1ppZFakJVqPE130_assertion SIO_000772 19154522 NP470683.RA0d9og_cAcbvrp17L8kC9sDZnHRldGgR1ppZFakJVqPE130_provenance.
- NP470683.RA0d9og_cAcbvrp17L8kC9sDZnHRldGgR1ppZFakJVqPE130_assertion wasDerivedFrom befree-20150227 NP470683.RA0d9og_cAcbvrp17L8kC9sDZnHRldGgR1ppZFakJVqPE130_provenance.
- NP470683.RA0d9og_cAcbvrp17L8kC9sDZnHRldGgR1ppZFakJVqPE130_assertion wasGeneratedBy ECO_0000203 NP470683.RA0d9og_cAcbvrp17L8kC9sDZnHRldGgR1ppZFakJVqPE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP470683.RA0d9og_cAcbvrp17L8kC9sDZnHRldGgR1ppZFakJVqPE130_provenance.