Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP719992.RA3dVTJmAJ99u9Og4C30iJiy3yspT5gfqfyQ5M8toRDGc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP719992.RA3dVTJmAJ99u9Og4C30iJiy3yspT5gfqfyQ5M8toRDGc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP719992.RA3dVTJmAJ99u9Og4C30iJiy3yspT5gfqfyQ5M8toRDGc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP719992.RA3dVTJmAJ99u9Og4C30iJiy3yspT5gfqfyQ5M8toRDGc130_provenance.
- NP719992.RA3dVTJmAJ99u9Og4C30iJiy3yspT5gfqfyQ5M8toRDGc130_assertion description "[STXBP1 (MUNC18.1), encoding syntaxin binding protein 1, has been reported in Ohtahara syndrome, a rare epileptic encephalopathy with suppression burst pattern on EEG, in patients with infantile spasms and in a few patients with nonsyndromic mental retardation without epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719992.RA3dVTJmAJ99u9Og4C30iJiy3yspT5gfqfyQ5M8toRDGc130_provenance.
- NP719992.RA3dVTJmAJ99u9Og4C30iJiy3yspT5gfqfyQ5M8toRDGc130_assertion evidence source_evidence_literature NP719992.RA3dVTJmAJ99u9Og4C30iJiy3yspT5gfqfyQ5M8toRDGc130_provenance.
- NP719992.RA3dVTJmAJ99u9Og4C30iJiy3yspT5gfqfyQ5M8toRDGc130_assertion SIO_000772 24095819 NP719992.RA3dVTJmAJ99u9Og4C30iJiy3yspT5gfqfyQ5M8toRDGc130_provenance.
- NP719992.RA3dVTJmAJ99u9Og4C30iJiy3yspT5gfqfyQ5M8toRDGc130_assertion wasDerivedFrom befree-20150227 NP719992.RA3dVTJmAJ99u9Og4C30iJiy3yspT5gfqfyQ5M8toRDGc130_provenance.
- NP719992.RA3dVTJmAJ99u9Og4C30iJiy3yspT5gfqfyQ5M8toRDGc130_assertion wasGeneratedBy ECO_0000203 NP719992.RA3dVTJmAJ99u9Og4C30iJiy3yspT5gfqfyQ5M8toRDGc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP719992.RA3dVTJmAJ99u9Og4C30iJiy3yspT5gfqfyQ5M8toRDGc130_provenance.