Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP198469.RA_1dzZJkfZ56FiG2nUYGTa1RtUcArwsqKRCZZ1dyJu_M130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP198469.RA_1dzZJkfZ56FiG2nUYGTa1RtUcArwsqKRCZZ1dyJu_M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP198469.RA_1dzZJkfZ56FiG2nUYGTa1RtUcArwsqKRCZZ1dyJu_M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP198469.RA_1dzZJkfZ56FiG2nUYGTa1RtUcArwsqKRCZZ1dyJu_M130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP198469.RA_1dzZJkfZ56FiG2nUYGTa1RtUcArwsqKRCZZ1dyJu_M130_provenance.
- NP198469.RA_1dzZJkfZ56FiG2nUYGTa1RtUcArwsqKRCZZ1dyJu_M130_assertion wasGeneratedBy ECO_0000203 NP198469.RA_1dzZJkfZ56FiG2nUYGTa1RtUcArwsqKRCZZ1dyJu_M130_provenance.
- NP198469.RA_1dzZJkfZ56FiG2nUYGTa1RtUcArwsqKRCZZ1dyJu_M130_assertion wasDerivedFrom lhgdn-20090331 NP198469.RA_1dzZJkfZ56FiG2nUYGTa1RtUcArwsqKRCZZ1dyJu_M130_provenance.
- NP198469.RA_1dzZJkfZ56FiG2nUYGTa1RtUcArwsqKRCZZ1dyJu_M130_assertion SIO_000772 12610651 NP198469.RA_1dzZJkfZ56FiG2nUYGTa1RtUcArwsqKRCZZ1dyJu_M130_provenance.
- NP198469.RA_1dzZJkfZ56FiG2nUYGTa1RtUcArwsqKRCZZ1dyJu_M130_assertion evidence source_evidence_literature NP198469.RA_1dzZJkfZ56FiG2nUYGTa1RtUcArwsqKRCZZ1dyJu_M130_provenance.
- NP198469.RA_1dzZJkfZ56FiG2nUYGTa1RtUcArwsqKRCZZ1dyJu_M130_assertion description "[R542Q in SCN1A was observed in one autism family and had previously been identified in a patient with juvenile myoclonic epilepsy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198469.RA_1dzZJkfZ56FiG2nUYGTa1RtUcArwsqKRCZZ1dyJu_M130_provenance.