Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP140509.RALyNsN0yT6QqIhh4CfVXO2nCFq1NEEv6z7jD5IAI579w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP140509.RALyNsN0yT6QqIhh4CfVXO2nCFq1NEEv6z7jD5IAI579w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP140509.RALyNsN0yT6QqIhh4CfVXO2nCFq1NEEv6z7jD5IAI579w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP140509.RALyNsN0yT6QqIhh4CfVXO2nCFq1NEEv6z7jD5IAI579w130_provenance.
- NP140509.RALyNsN0yT6QqIhh4CfVXO2nCFq1NEEv6z7jD5IAI579w130_assertion description "[We genotyped the EPO rS1617640 SNP in 189 patients with MDS, 257 with acute myeloid leukemia (AML), 106 with acute lymphoblastic leukemia, 97 with chronic lymphocytic leukemia, 353 with chronic myeloid leukemia, and 95 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP140509.RALyNsN0yT6QqIhh4CfVXO2nCFq1NEEv6z7jD5IAI579w130_provenance.
- NP140509.RALyNsN0yT6QqIhh4CfVXO2nCFq1NEEv6z7jD5IAI579w130_assertion evidence source_evidence_literature NP140509.RALyNsN0yT6QqIhh4CfVXO2nCFq1NEEv6z7jD5IAI579w130_provenance.
- NP140509.RALyNsN0yT6QqIhh4CfVXO2nCFq1NEEv6z7jD5IAI579w130_assertion SIO_000772 21078205 NP140509.RALyNsN0yT6QqIhh4CfVXO2nCFq1NEEv6z7jD5IAI579w130_provenance.
- NP140509.RALyNsN0yT6QqIhh4CfVXO2nCFq1NEEv6z7jD5IAI579w130_assertion wasDerivedFrom gad-20150221 NP140509.RALyNsN0yT6QqIhh4CfVXO2nCFq1NEEv6z7jD5IAI579w130_provenance.
- NP140509.RALyNsN0yT6QqIhh4CfVXO2nCFq1NEEv6z7jD5IAI579w130_assertion wasGeneratedBy ECO_0000203 NP140509.RALyNsN0yT6QqIhh4CfVXO2nCFq1NEEv6z7jD5IAI579w130_provenance.
- gad-20150221 importedOn "2015-02-21" NP140509.RALyNsN0yT6QqIhh4CfVXO2nCFq1NEEv6z7jD5IAI579w130_provenance.