Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP189960.RA6WcT1UNdheF1WxNbTHBXSnFO3n9zvNghiXbdVadPCZ4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP189960.RA6WcT1UNdheF1WxNbTHBXSnFO3n9zvNghiXbdVadPCZ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP189960.RA6WcT1UNdheF1WxNbTHBXSnFO3n9zvNghiXbdVadPCZ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP189960.RA6WcT1UNdheF1WxNbTHBXSnFO3n9zvNghiXbdVadPCZ4130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP189960.RA6WcT1UNdheF1WxNbTHBXSnFO3n9zvNghiXbdVadPCZ4130_provenance.
- NP189960.RA6WcT1UNdheF1WxNbTHBXSnFO3n9zvNghiXbdVadPCZ4130_assertion wasGeneratedBy ECO_0000203 NP189960.RA6WcT1UNdheF1WxNbTHBXSnFO3n9zvNghiXbdVadPCZ4130_provenance.
- NP189960.RA6WcT1UNdheF1WxNbTHBXSnFO3n9zvNghiXbdVadPCZ4130_assertion wasDerivedFrom lhgdn-20090331 NP189960.RA6WcT1UNdheF1WxNbTHBXSnFO3n9zvNghiXbdVadPCZ4130_provenance.
- NP189960.RA6WcT1UNdheF1WxNbTHBXSnFO3n9zvNghiXbdVadPCZ4130_assertion SIO_000772 18060736 NP189960.RA6WcT1UNdheF1WxNbTHBXSnFO3n9zvNghiXbdVadPCZ4130_provenance.
- NP189960.RA6WcT1UNdheF1WxNbTHBXSnFO3n9zvNghiXbdVadPCZ4130_assertion evidence source_evidence_literature NP189960.RA6WcT1UNdheF1WxNbTHBXSnFO3n9zvNghiXbdVadPCZ4130_provenance.
- NP189960.RA6WcT1UNdheF1WxNbTHBXSnFO3n9zvNghiXbdVadPCZ4130_assertion description "[rare mutations in the DOCK8 gene may contribute to some cases of autosomal dominant mental retardation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP189960.RA6WcT1UNdheF1WxNbTHBXSnFO3n9zvNghiXbdVadPCZ4130_provenance.