Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP683300.RAc1fNsEDA_f8TvpmhkHn2v5oou42CgjxsqaNe20OH3b8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP683300.RAc1fNsEDA_f8TvpmhkHn2v5oou42CgjxsqaNe20OH3b8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683300.RAc1fNsEDA_f8TvpmhkHn2v5oou42CgjxsqaNe20OH3b8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683300.RAc1fNsEDA_f8TvpmhkHn2v5oou42CgjxsqaNe20OH3b8130_provenance.
- NP683300.RAc1fNsEDA_f8TvpmhkHn2v5oou42CgjxsqaNe20OH3b8130_assertion description "[Together with previous reports, our study further indicates that genetic testing of SCN8A should be considered in children with unclassified severe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683300.RAc1fNsEDA_f8TvpmhkHn2v5oou42CgjxsqaNe20OH3b8130_provenance.
- NP683300.RAc1fNsEDA_f8TvpmhkHn2v5oou42CgjxsqaNe20OH3b8130_assertion evidence source_evidence_literature NP683300.RAc1fNsEDA_f8TvpmhkHn2v5oou42CgjxsqaNe20OH3b8130_provenance.
- NP683300.RAc1fNsEDA_f8TvpmhkHn2v5oou42CgjxsqaNe20OH3b8130_assertion SIO_000772 24888894 NP683300.RAc1fNsEDA_f8TvpmhkHn2v5oou42CgjxsqaNe20OH3b8130_provenance.
- NP683300.RAc1fNsEDA_f8TvpmhkHn2v5oou42CgjxsqaNe20OH3b8130_assertion wasDerivedFrom befree-20150227 NP683300.RAc1fNsEDA_f8TvpmhkHn2v5oou42CgjxsqaNe20OH3b8130_provenance.
- NP683300.RAc1fNsEDA_f8TvpmhkHn2v5oou42CgjxsqaNe20OH3b8130_assertion wasGeneratedBy ECO_0000203 NP683300.RAc1fNsEDA_f8TvpmhkHn2v5oou42CgjxsqaNe20OH3b8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP683300.RAc1fNsEDA_f8TvpmhkHn2v5oou42CgjxsqaNe20OH3b8130_provenance.