Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1360292.RAnbpZe40-ZdW6oNi3HDVtKaKuGSKdu-S2Bd7F2lcaObg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1360292.RAnbpZe40-ZdW6oNi3HDVtKaKuGSKdu-S2Bd7F2lcaObg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1360292.RAnbpZe40-ZdW6oNi3HDVtKaKuGSKdu-S2Bd7F2lcaObg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1360292.RAnbpZe40-ZdW6oNi3HDVtKaKuGSKdu-S2Bd7F2lcaObg130_provenance.
- NP1360292.RAnbpZe40-ZdW6oNi3HDVtKaKuGSKdu-S2Bd7F2lcaObg130_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." NP1360292.RAnbpZe40-ZdW6oNi3HDVtKaKuGSKdu-S2Bd7F2lcaObg130_provenance.
- NP1360292.RAnbpZe40-ZdW6oNi3HDVtKaKuGSKdu-S2Bd7F2lcaObg130_assertion evidence source_evidence_literature NP1360292.RAnbpZe40-ZdW6oNi3HDVtKaKuGSKdu-S2Bd7F2lcaObg130_provenance.
- NP1360292.RAnbpZe40-ZdW6oNi3HDVtKaKuGSKdu-S2Bd7F2lcaObg130_assertion SIO_000772 8871944 NP1360292.RAnbpZe40-ZdW6oNi3HDVtKaKuGSKdu-S2Bd7F2lcaObg130_provenance.
- NP1360292.RAnbpZe40-ZdW6oNi3HDVtKaKuGSKdu-S2Bd7F2lcaObg130_assertion wasDerivedFrom befree-2016 NP1360292.RAnbpZe40-ZdW6oNi3HDVtKaKuGSKdu-S2Bd7F2lcaObg130_provenance.
- NP1360292.RAnbpZe40-ZdW6oNi3HDVtKaKuGSKdu-S2Bd7F2lcaObg130_assertion wasGeneratedBy ECO_0000203 NP1360292.RAnbpZe40-ZdW6oNi3HDVtKaKuGSKdu-S2Bd7F2lcaObg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1360292.RAnbpZe40-ZdW6oNi3HDVtKaKuGSKdu-S2Bd7F2lcaObg130_provenance.