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- source_evidence_literature type ECO_0000212 NP978271.RAm0iqGe9lCWswVN8XG6GaCCDoTHsQHoIaAp8wxJLaBcA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978271.RAm0iqGe9lCWswVN8XG6GaCCDoTHsQHoIaAp8wxJLaBcA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978271.RAm0iqGe9lCWswVN8XG6GaCCDoTHsQHoIaAp8wxJLaBcA130_provenance.
- NP978271.RAm0iqGe9lCWswVN8XG6GaCCDoTHsQHoIaAp8wxJLaBcA130_assertion description "[Based on the association analysis results in a previously identified linkage region, we propose that HTR3C represents a novel candidate locus for ASDs and should be tested in other populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978271.RAm0iqGe9lCWswVN8XG6GaCCDoTHsQHoIaAp8wxJLaBcA130_provenance.
- NP978271.RAm0iqGe9lCWswVN8XG6GaCCDoTHsQHoIaAp8wxJLaBcA130_assertion evidence source_evidence_literature NP978271.RAm0iqGe9lCWswVN8XG6GaCCDoTHsQHoIaAp8wxJLaBcA130_provenance.
- NP978271.RAm0iqGe9lCWswVN8XG6GaCCDoTHsQHoIaAp8wxJLaBcA130_assertion SIO_000772 19035560 NP978271.RAm0iqGe9lCWswVN8XG6GaCCDoTHsQHoIaAp8wxJLaBcA130_provenance.
- NP978271.RAm0iqGe9lCWswVN8XG6GaCCDoTHsQHoIaAp8wxJLaBcA130_assertion wasDerivedFrom befree-20150227 NP978271.RAm0iqGe9lCWswVN8XG6GaCCDoTHsQHoIaAp8wxJLaBcA130_provenance.
- NP978271.RAm0iqGe9lCWswVN8XG6GaCCDoTHsQHoIaAp8wxJLaBcA130_assertion wasGeneratedBy ECO_0000203 NP978271.RAm0iqGe9lCWswVN8XG6GaCCDoTHsQHoIaAp8wxJLaBcA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978271.RAm0iqGe9lCWswVN8XG6GaCCDoTHsQHoIaAp8wxJLaBcA130_provenance.