Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_provenance.
- NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_assertion wasGeneratedBy ECO_0000203 NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_provenance.
- NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_assertion wasDerivedFrom befree-20150227 NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_provenance.
- NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_assertion SIO_000772 22216833 NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_provenance.
- NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_assertion evidence source_evidence_literature NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_provenance.
- NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_assertion description "[There are several candidate genes within the SRO, including CYP11A1, SEMA7A, CPLX3, ARID3B, STRA6, SIN3A and CSK, that may predispose to many of the clinical features observed in individuals with 15q24 deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_provenance.