Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP478033.RAYTahZHSbV_LwLYqx0VN6QiR7EXln6EIEBzedjAMBmao130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478033.RAYTahZHSbV_LwLYqx0VN6QiR7EXln6EIEBzedjAMBmao130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478033.RAYTahZHSbV_LwLYqx0VN6QiR7EXln6EIEBzedjAMBmao130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478033.RAYTahZHSbV_LwLYqx0VN6QiR7EXln6EIEBzedjAMBmao130_provenance.
- NP478033.RAYTahZHSbV_LwLYqx0VN6QiR7EXln6EIEBzedjAMBmao130_assertion description "[We confirmed the finding of an increased frequency of the C4B null allele in autism and found that the related disorders also had an increased frequency of this null allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478033.RAYTahZHSbV_LwLYqx0VN6QiR7EXln6EIEBzedjAMBmao130_provenance.
- NP478033.RAYTahZHSbV_LwLYqx0VN6QiR7EXln6EIEBzedjAMBmao130_assertion evidence source_evidence_literature NP478033.RAYTahZHSbV_LwLYqx0VN6QiR7EXln6EIEBzedjAMBmao130_provenance.
- NP478033.RAYTahZHSbV_LwLYqx0VN6QiR7EXln6EIEBzedjAMBmao130_assertion SIO_000772 8871944 NP478033.RAYTahZHSbV_LwLYqx0VN6QiR7EXln6EIEBzedjAMBmao130_provenance.
- NP478033.RAYTahZHSbV_LwLYqx0VN6QiR7EXln6EIEBzedjAMBmao130_assertion wasDerivedFrom befree-20140225 NP478033.RAYTahZHSbV_LwLYqx0VN6QiR7EXln6EIEBzedjAMBmao130_provenance.
- NP478033.RAYTahZHSbV_LwLYqx0VN6QiR7EXln6EIEBzedjAMBmao130_assertion wasGeneratedBy ECO_0000203 NP478033.RAYTahZHSbV_LwLYqx0VN6QiR7EXln6EIEBzedjAMBmao130_provenance.
- befree-20140225 importedOn "2014-02-25" NP478033.RAYTahZHSbV_LwLYqx0VN6QiR7EXln6EIEBzedjAMBmao130_provenance.