Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP478033.RAYTahZHSbV_LwLYqx0VN6QiR7EXln6EIEBzedjAMBmao130_assertion> ?p ?o ?g. }
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- NP478033.RAYTahZHSbV_LwLYqx0VN6QiR7EXln6EIEBzedjAMBmao130_assertion type Assertion NP478033.RAYTahZHSbV_LwLYqx0VN6QiR7EXln6EIEBzedjAMBmao130_head.
- 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.