Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP964423.RA5y7v1ssGzePHGF0IunhdeC3F3qMLyaJyd2KQ-BvE5Rc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP964423.RA5y7v1ssGzePHGF0IunhdeC3F3qMLyaJyd2KQ-BvE5Rc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP964423.RA5y7v1ssGzePHGF0IunhdeC3F3qMLyaJyd2KQ-BvE5Rc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP964423.RA5y7v1ssGzePHGF0IunhdeC3F3qMLyaJyd2KQ-BvE5Rc130_provenance.
- NP964423.RA5y7v1ssGzePHGF0IunhdeC3F3qMLyaJyd2KQ-BvE5Rc130_assertion description "[Our latest studies, as well as those by Whitehouse et al., show that not all families with JME have their genetic locus in chromosome 6p, and that childhood absence epilepsy does not map to the same EJM1 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP964423.RA5y7v1ssGzePHGF0IunhdeC3F3qMLyaJyd2KQ-BvE5Rc130_provenance.
- NP964423.RA5y7v1ssGzePHGF0IunhdeC3F3qMLyaJyd2KQ-BvE5Rc130_assertion evidence source_evidence_literature NP964423.RA5y7v1ssGzePHGF0IunhdeC3F3qMLyaJyd2KQ-BvE5Rc130_provenance.
- NP964423.RA5y7v1ssGzePHGF0IunhdeC3F3qMLyaJyd2KQ-BvE5Rc130_assertion SIO_000772 8293722 NP964423.RA5y7v1ssGzePHGF0IunhdeC3F3qMLyaJyd2KQ-BvE5Rc130_provenance.
- NP964423.RA5y7v1ssGzePHGF0IunhdeC3F3qMLyaJyd2KQ-BvE5Rc130_assertion wasDerivedFrom befree-20150227 NP964423.RA5y7v1ssGzePHGF0IunhdeC3F3qMLyaJyd2KQ-BvE5Rc130_provenance.
- NP964423.RA5y7v1ssGzePHGF0IunhdeC3F3qMLyaJyd2KQ-BvE5Rc130_assertion wasGeneratedBy ECO_0000203 NP964423.RA5y7v1ssGzePHGF0IunhdeC3F3qMLyaJyd2KQ-BvE5Rc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP964423.RA5y7v1ssGzePHGF0IunhdeC3F3qMLyaJyd2KQ-BvE5Rc130_provenance.