Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1357068.RA6FTNSujiR-PH-VOtQmL9NspiQwrHBvWMhLmyESw5Mqc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1357068.RA6FTNSujiR-PH-VOtQmL9NspiQwrHBvWMhLmyESw5Mqc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1357068.RA6FTNSujiR-PH-VOtQmL9NspiQwrHBvWMhLmyESw5Mqc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1357068.RA6FTNSujiR-PH-VOtQmL9NspiQwrHBvWMhLmyESw5Mqc130_provenance.
- NP1357068.RA6FTNSujiR-PH-VOtQmL9NspiQwrHBvWMhLmyESw5Mqc130_assertion description "[Susceptibility genes for two syndromes of idiopathic generalized epilepsies, the benign familial neonatal convulsions and juvenile myoclonic epilepsy, have been assigned to the chromosomal regions 20q13 (EBN1), 8q24 (EBN2) and 6p21 (EJM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1357068.RA6FTNSujiR-PH-VOtQmL9NspiQwrHBvWMhLmyESw5Mqc130_provenance.
- NP1357068.RA6FTNSujiR-PH-VOtQmL9NspiQwrHBvWMhLmyESw5Mqc130_assertion evidence source_evidence_literature NP1357068.RA6FTNSujiR-PH-VOtQmL9NspiQwrHBvWMhLmyESw5Mqc130_provenance.
- NP1357068.RA6FTNSujiR-PH-VOtQmL9NspiQwrHBvWMhLmyESw5Mqc130_assertion SIO_000772 8796880 NP1357068.RA6FTNSujiR-PH-VOtQmL9NspiQwrHBvWMhLmyESw5Mqc130_provenance.
- NP1357068.RA6FTNSujiR-PH-VOtQmL9NspiQwrHBvWMhLmyESw5Mqc130_assertion wasDerivedFrom befree-2016 NP1357068.RA6FTNSujiR-PH-VOtQmL9NspiQwrHBvWMhLmyESw5Mqc130_provenance.
- NP1357068.RA6FTNSujiR-PH-VOtQmL9NspiQwrHBvWMhLmyESw5Mqc130_assertion wasGeneratedBy ECO_0000203 NP1357068.RA6FTNSujiR-PH-VOtQmL9NspiQwrHBvWMhLmyESw5Mqc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1357068.RA6FTNSujiR-PH-VOtQmL9NspiQwrHBvWMhLmyESw5Mqc130_provenance.