Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP770653.RANlOupQjZG5RrB9LzEo2aswV-x9BBSN4Q5R703Jl6QgA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP770653.RANlOupQjZG5RrB9LzEo2aswV-x9BBSN4Q5R703Jl6QgA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP770653.RANlOupQjZG5RrB9LzEo2aswV-x9BBSN4Q5R703Jl6QgA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP770653.RANlOupQjZG5RrB9LzEo2aswV-x9BBSN4Q5R703Jl6QgA130_provenance.
- NP770653.RANlOupQjZG5RrB9LzEo2aswV-x9BBSN4Q5R703Jl6QgA130_assertion description "[Polymorphism located between CPT1B and CHKB, and HLA-DRB1*1501-DQB1*0602 haplotype confer susceptibility to CNS hypersomnias (essential hypersomnia).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP770653.RANlOupQjZG5RrB9LzEo2aswV-x9BBSN4Q5R703Jl6QgA130_provenance.
- NP770653.RANlOupQjZG5RrB9LzEo2aswV-x9BBSN4Q5R703Jl6QgA130_assertion evidence source_evidence_literature NP770653.RANlOupQjZG5RrB9LzEo2aswV-x9BBSN4Q5R703Jl6QgA130_provenance.
- NP770653.RANlOupQjZG5RrB9LzEo2aswV-x9BBSN4Q5R703Jl6QgA130_assertion SIO_000772 19404393 NP770653.RANlOupQjZG5RrB9LzEo2aswV-x9BBSN4Q5R703Jl6QgA130_provenance.
- NP770653.RANlOupQjZG5RrB9LzEo2aswV-x9BBSN4Q5R703Jl6QgA130_assertion wasDerivedFrom befree-20140225 NP770653.RANlOupQjZG5RrB9LzEo2aswV-x9BBSN4Q5R703Jl6QgA130_provenance.
- NP770653.RANlOupQjZG5RrB9LzEo2aswV-x9BBSN4Q5R703Jl6QgA130_assertion wasGeneratedBy ECO_0000203 NP770653.RANlOupQjZG5RrB9LzEo2aswV-x9BBSN4Q5R703Jl6QgA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP770653.RANlOupQjZG5RrB9LzEo2aswV-x9BBSN4Q5R703Jl6QgA130_provenance.