Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP350669.RAwmVklgzG7fzyXNXJ51xaEp8ZuxpCIyMcOEtIUBQ7i6k130_assertion> ?p ?o ?g. }
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- NP350669.RAwmVklgzG7fzyXNXJ51xaEp8ZuxpCIyMcOEtIUBQ7i6k130_assertion type Assertion NP350669.RAwmVklgzG7fzyXNXJ51xaEp8ZuxpCIyMcOEtIUBQ7i6k130_head.
- NP350669.RAwmVklgzG7fzyXNXJ51xaEp8ZuxpCIyMcOEtIUBQ7i6k130_assertion wasGeneratedBy ECO_0000203 NP350669.RAwmVklgzG7fzyXNXJ51xaEp8ZuxpCIyMcOEtIUBQ7i6k130_provenance.
- NP350669.RAwmVklgzG7fzyXNXJ51xaEp8ZuxpCIyMcOEtIUBQ7i6k130_assertion wasDerivedFrom befree-20150227 NP350669.RAwmVklgzG7fzyXNXJ51xaEp8ZuxpCIyMcOEtIUBQ7i6k130_provenance.
- NP350669.RAwmVklgzG7fzyXNXJ51xaEp8ZuxpCIyMcOEtIUBQ7i6k130_assertion SIO_000772 12838518 NP350669.RAwmVklgzG7fzyXNXJ51xaEp8ZuxpCIyMcOEtIUBQ7i6k130_provenance.
- NP350669.RAwmVklgzG7fzyXNXJ51xaEp8ZuxpCIyMcOEtIUBQ7i6k130_assertion evidence source_evidence_literature NP350669.RAwmVklgzG7fzyXNXJ51xaEp8ZuxpCIyMcOEtIUBQ7i6k130_provenance.
- NP350669.RAwmVklgzG7fzyXNXJ51xaEp8ZuxpCIyMcOEtIUBQ7i6k130_assertion description "[Missense DCX mutations may manifest as non-syndromic mental retardation with cryptogenic epilepsy in female subjects and SBH in boys.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP350669.RAwmVklgzG7fzyXNXJ51xaEp8ZuxpCIyMcOEtIUBQ7i6k130_provenance.