Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the 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.
- NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_assertion evidence source_evidence_literature NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_provenance.
- NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_assertion SIO_000772 23161826 NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_provenance.
- NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_assertion wasDerivedFrom befree-20140225 NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_provenance.
- NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_assertion wasGeneratedBy ECO_0000203 NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP273335.RAdH_qkMZCZyu8wwd-8rAOmvBAtQ5WgD2tm4FU4zFRSUc130_provenance.