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- source_evidence_literature type ECO_0000212 NP427853.RAPkW20B1X937B-x8HC7orApUww_cp1MTYPBGUR67Er_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP427853.RAPkW20B1X937B-x8HC7orApUww_cp1MTYPBGUR67Er_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP427853.RAPkW20B1X937B-x8HC7orApUww_cp1MTYPBGUR67Er_s130_provenance.
- NP427853.RAPkW20B1X937B-x8HC7orApUww_cp1MTYPBGUR67Er_s130_assertion description "[The highly significant association of C4AQ0 with SLE across multiple HLA haplotypes and ethnic groups, and the presence of different mechanisms leading to a C4A protein deficiency among SLE patients suggested that deficiency or low expression level of C4A protein is a primary risk factor for SLE disease susceptibility per se.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427853.RAPkW20B1X937B-x8HC7orApUww_cp1MTYPBGUR67Er_s130_provenance.
- NP427853.RAPkW20B1X937B-x8HC7orApUww_cp1MTYPBGUR67Er_s130_assertion evidence source_evidence_literature NP427853.RAPkW20B1X937B-x8HC7orApUww_cp1MTYPBGUR67Er_s130_provenance.
- NP427853.RAPkW20B1X937B-x8HC7orApUww_cp1MTYPBGUR67Er_s130_assertion SIO_000772 14719377 NP427853.RAPkW20B1X937B-x8HC7orApUww_cp1MTYPBGUR67Er_s130_provenance.
- NP427853.RAPkW20B1X937B-x8HC7orApUww_cp1MTYPBGUR67Er_s130_assertion wasDerivedFrom befree-2016 NP427853.RAPkW20B1X937B-x8HC7orApUww_cp1MTYPBGUR67Er_s130_provenance.
- NP427853.RAPkW20B1X937B-x8HC7orApUww_cp1MTYPBGUR67Er_s130_assertion wasGeneratedBy ECO_0000203 NP427853.RAPkW20B1X937B-x8HC7orApUww_cp1MTYPBGUR67Er_s130_provenance.
- befree-2016 importedOn "2016-02-19" NP427853.RAPkW20B1X937B-x8HC7orApUww_cp1MTYPBGUR67Er_s130_provenance.