Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP326139.RAIpXUdz427dGbYcQhLMFZioh9DlE6uFAgL9TxVJ5LXpY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP326139.RAIpXUdz427dGbYcQhLMFZioh9DlE6uFAgL9TxVJ5LXpY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP326139.RAIpXUdz427dGbYcQhLMFZioh9DlE6uFAgL9TxVJ5LXpY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP326139.RAIpXUdz427dGbYcQhLMFZioh9DlE6uFAgL9TxVJ5LXpY130_provenance.
- NP326139.RAIpXUdz427dGbYcQhLMFZioh9DlE6uFAgL9TxVJ5LXpY130_assertion description "[In this study, we tested whether null genotypes for the GSTM1 and GSTT1 genes altered the risks for MDS, AML and AA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP326139.RAIpXUdz427dGbYcQhLMFZioh9DlE6uFAgL9TxVJ5LXpY130_provenance.
- NP326139.RAIpXUdz427dGbYcQhLMFZioh9DlE6uFAgL9TxVJ5LXpY130_assertion evidence source_evidence_literature NP326139.RAIpXUdz427dGbYcQhLMFZioh9DlE6uFAgL9TxVJ5LXpY130_provenance.
- NP326139.RAIpXUdz427dGbYcQhLMFZioh9DlE6uFAgL9TxVJ5LXpY130_assertion SIO_000772 11488937 NP326139.RAIpXUdz427dGbYcQhLMFZioh9DlE6uFAgL9TxVJ5LXpY130_provenance.
- NP326139.RAIpXUdz427dGbYcQhLMFZioh9DlE6uFAgL9TxVJ5LXpY130_assertion wasDerivedFrom befree-2016 NP326139.RAIpXUdz427dGbYcQhLMFZioh9DlE6uFAgL9TxVJ5LXpY130_provenance.
- NP326139.RAIpXUdz427dGbYcQhLMFZioh9DlE6uFAgL9TxVJ5LXpY130_assertion wasGeneratedBy ECO_0000203 NP326139.RAIpXUdz427dGbYcQhLMFZioh9DlE6uFAgL9TxVJ5LXpY130_provenance.
- befree-2016 importedOn "2016-02-19" NP326139.RAIpXUdz427dGbYcQhLMFZioh9DlE6uFAgL9TxVJ5LXpY130_provenance.