Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP822843.RAH7E_rs-SQT8wjDSHYRnAB1U0K4WbsSDc4qnUJnK-u8Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP822843.RAH7E_rs-SQT8wjDSHYRnAB1U0K4WbsSDc4qnUJnK-u8Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP822843.RAH7E_rs-SQT8wjDSHYRnAB1U0K4WbsSDc4qnUJnK-u8Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP822843.RAH7E_rs-SQT8wjDSHYRnAB1U0K4WbsSDc4qnUJnK-u8Y130_provenance.
- NP822843.RAH7E_rs-SQT8wjDSHYRnAB1U0K4WbsSDc4qnUJnK-u8Y130_assertion description "[Copy number variations in regulators of complement activation genes (CFHR1 and CFHR3) and glutathione S transferase genes (GSTM1 and GSTT1) have been associated with AMD, and several additional loci have been identified as regions of potential interest but require further evaluation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822843.RAH7E_rs-SQT8wjDSHYRnAB1U0K4WbsSDc4qnUJnK-u8Y130_provenance.
- NP822843.RAH7E_rs-SQT8wjDSHYRnAB1U0K4WbsSDc4qnUJnK-u8Y130_assertion evidence source_evidence_literature NP822843.RAH7E_rs-SQT8wjDSHYRnAB1U0K4WbsSDc4qnUJnK-u8Y130_provenance.
- NP822843.RAH7E_rs-SQT8wjDSHYRnAB1U0K4WbsSDc4qnUJnK-u8Y130_assertion SIO_000772 23244519 NP822843.RAH7E_rs-SQT8wjDSHYRnAB1U0K4WbsSDc4qnUJnK-u8Y130_provenance.
- NP822843.RAH7E_rs-SQT8wjDSHYRnAB1U0K4WbsSDc4qnUJnK-u8Y130_assertion wasDerivedFrom befree-20140225 NP822843.RAH7E_rs-SQT8wjDSHYRnAB1U0K4WbsSDc4qnUJnK-u8Y130_provenance.
- NP822843.RAH7E_rs-SQT8wjDSHYRnAB1U0K4WbsSDc4qnUJnK-u8Y130_assertion wasGeneratedBy ECO_0000203 NP822843.RAH7E_rs-SQT8wjDSHYRnAB1U0K4WbsSDc4qnUJnK-u8Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP822843.RAH7E_rs-SQT8wjDSHYRnAB1U0K4WbsSDc4qnUJnK-u8Y130_provenance.