Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_assertion> ?p ?o ?g. }
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- NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_assertion type Assertion NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_head.
- NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_assertion wasGeneratedBy ECO_0000203 NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_provenance.
- NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_assertion wasDerivedFrom befree-20140225 NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_provenance.
- NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_assertion SIO_000772 23161826 NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_provenance.
- NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_assertion evidence source_evidence_literature NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_provenance.
- NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_assertion description "[De novo mutations in SYNGAP1, which codes for a RAS/RAP GTP-activating protein, cause nonsyndromic intellectual disability (NSID).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_provenance.