Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP350653.RA3iOHYTBlAlM7H8m3cocJerX2NKqzdx68E0pfqXbwWZ0130_assertion> ?p ?o ?g. }
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- NP350653.RA3iOHYTBlAlM7H8m3cocJerX2NKqzdx68E0pfqXbwWZ0130_assertion type Assertion NP350653.RA3iOHYTBlAlM7H8m3cocJerX2NKqzdx68E0pfqXbwWZ0130_head.
- NP350653.RA3iOHYTBlAlM7H8m3cocJerX2NKqzdx68E0pfqXbwWZ0130_assertion description "[In human patients, cortical dysplasia produced by Doublecortin (DCX) mutations lead to mental retardation and intractable infantile epilepsies, but the underlying mechanisms are not known.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP350653.RA3iOHYTBlAlM7H8m3cocJerX2NKqzdx68E0pfqXbwWZ0130_provenance.
- NP350653.RA3iOHYTBlAlM7H8m3cocJerX2NKqzdx68E0pfqXbwWZ0130_assertion evidence source_evidence_literature NP350653.RA3iOHYTBlAlM7H8m3cocJerX2NKqzdx68E0pfqXbwWZ0130_provenance.
- NP350653.RA3iOHYTBlAlM7H8m3cocJerX2NKqzdx68E0pfqXbwWZ0130_assertion SIO_000772 19144832 NP350653.RA3iOHYTBlAlM7H8m3cocJerX2NKqzdx68E0pfqXbwWZ0130_provenance.
- NP350653.RA3iOHYTBlAlM7H8m3cocJerX2NKqzdx68E0pfqXbwWZ0130_assertion wasDerivedFrom befree-20150227 NP350653.RA3iOHYTBlAlM7H8m3cocJerX2NKqzdx68E0pfqXbwWZ0130_provenance.
- NP350653.RA3iOHYTBlAlM7H8m3cocJerX2NKqzdx68E0pfqXbwWZ0130_assertion wasGeneratedBy ECO_0000203 NP350653.RA3iOHYTBlAlM7H8m3cocJerX2NKqzdx68E0pfqXbwWZ0130_provenance.