Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_provenance.
- NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_assertion description "[By array comparative genomic hybridization (array-CGH), we identified a small duplication at Xq28 in a large family with a severe form of MR associated with progressive spasticity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_provenance.
- NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_assertion evidence source_evidence_literature NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_provenance.
- NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_assertion SIO_000772 16080119 NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_provenance.
- NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_assertion wasDerivedFrom befree-20140225 NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_provenance.
- NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_assertion wasGeneratedBy ECO_0000203 NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_provenance.