Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP201496.RA1xtsQFvt4UkSKC7YIdzZ8mp-21uFx8zG3CH_qQYL6_Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP201496.RA1xtsQFvt4UkSKC7YIdzZ8mp-21uFx8zG3CH_qQYL6_Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP201496.RA1xtsQFvt4UkSKC7YIdzZ8mp-21uFx8zG3CH_qQYL6_Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP201496.RA1xtsQFvt4UkSKC7YIdzZ8mp-21uFx8zG3CH_qQYL6_Y130_provenance.
- NP201496.RA1xtsQFvt4UkSKC7YIdzZ8mp-21uFx8zG3CH_qQYL6_Y130_assertion description "[Screening of the LGI4 coding region in BFIC and childhood absence epilepsy (CAE) revealed several frequent exonic polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP201496.RA1xtsQFvt4UkSKC7YIdzZ8mp-21uFx8zG3CH_qQYL6_Y130_provenance.
- NP201496.RA1xtsQFvt4UkSKC7YIdzZ8mp-21uFx8zG3CH_qQYL6_Y130_assertion evidence source_evidence_literature NP201496.RA1xtsQFvt4UkSKC7YIdzZ8mp-21uFx8zG3CH_qQYL6_Y130_provenance.
- NP201496.RA1xtsQFvt4UkSKC7YIdzZ8mp-21uFx8zG3CH_qQYL6_Y130_assertion SIO_000772 14505228 NP201496.RA1xtsQFvt4UkSKC7YIdzZ8mp-21uFx8zG3CH_qQYL6_Y130_provenance.
- NP201496.RA1xtsQFvt4UkSKC7YIdzZ8mp-21uFx8zG3CH_qQYL6_Y130_assertion wasDerivedFrom lhgdn-20090331 NP201496.RA1xtsQFvt4UkSKC7YIdzZ8mp-21uFx8zG3CH_qQYL6_Y130_provenance.
- NP201496.RA1xtsQFvt4UkSKC7YIdzZ8mp-21uFx8zG3CH_qQYL6_Y130_assertion wasGeneratedBy ECO_0000203 NP201496.RA1xtsQFvt4UkSKC7YIdzZ8mp-21uFx8zG3CH_qQYL6_Y130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP201496.RA1xtsQFvt4UkSKC7YIdzZ8mp-21uFx8zG3CH_qQYL6_Y130_provenance.