Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1013631.RAUEekxZEgs9SpQsws_rYHWlAwhpktPhpYyApQCnQ1utA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1013631.RAUEekxZEgs9SpQsws_rYHWlAwhpktPhpYyApQCnQ1utA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1013631.RAUEekxZEgs9SpQsws_rYHWlAwhpktPhpYyApQCnQ1utA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1013631.RAUEekxZEgs9SpQsws_rYHWlAwhpktPhpYyApQCnQ1utA130_provenance.
- NP1013631.RAUEekxZEgs9SpQsws_rYHWlAwhpktPhpYyApQCnQ1utA130_assertion description "[We previously reported that a deficient form of the C4B gene, termed the C4B null allele (no C4B protein produced) had an increased frequently in autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1013631.RAUEekxZEgs9SpQsws_rYHWlAwhpktPhpYyApQCnQ1utA130_provenance.
- NP1013631.RAUEekxZEgs9SpQsws_rYHWlAwhpktPhpYyApQCnQ1utA130_assertion evidence source_evidence_literature NP1013631.RAUEekxZEgs9SpQsws_rYHWlAwhpktPhpYyApQCnQ1utA130_provenance.
- NP1013631.RAUEekxZEgs9SpQsws_rYHWlAwhpktPhpYyApQCnQ1utA130_assertion SIO_000772 8871944 NP1013631.RAUEekxZEgs9SpQsws_rYHWlAwhpktPhpYyApQCnQ1utA130_provenance.
- NP1013631.RAUEekxZEgs9SpQsws_rYHWlAwhpktPhpYyApQCnQ1utA130_assertion wasDerivedFrom befree-20150227 NP1013631.RAUEekxZEgs9SpQsws_rYHWlAwhpktPhpYyApQCnQ1utA130_provenance.
- NP1013631.RAUEekxZEgs9SpQsws_rYHWlAwhpktPhpYyApQCnQ1utA130_assertion wasGeneratedBy ECO_0000203 NP1013631.RAUEekxZEgs9SpQsws_rYHWlAwhpktPhpYyApQCnQ1utA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1013631.RAUEekxZEgs9SpQsws_rYHWlAwhpktPhpYyApQCnQ1utA130_provenance.