Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP884930.RAMIVPgIGHSNV5Np3ezwJrnfzPGV0zByHhlni9fep_0To130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP884930.RAMIVPgIGHSNV5Np3ezwJrnfzPGV0zByHhlni9fep_0To130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP884930.RAMIVPgIGHSNV5Np3ezwJrnfzPGV0zByHhlni9fep_0To130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP884930.RAMIVPgIGHSNV5Np3ezwJrnfzPGV0zByHhlni9fep_0To130_provenance.
- NP884930.RAMIVPgIGHSNV5Np3ezwJrnfzPGV0zByHhlni9fep_0To130_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." NP884930.RAMIVPgIGHSNV5Np3ezwJrnfzPGV0zByHhlni9fep_0To130_provenance.
- NP884930.RAMIVPgIGHSNV5Np3ezwJrnfzPGV0zByHhlni9fep_0To130_assertion evidence source_evidence_literature NP884930.RAMIVPgIGHSNV5Np3ezwJrnfzPGV0zByHhlni9fep_0To130_provenance.
- NP884930.RAMIVPgIGHSNV5Np3ezwJrnfzPGV0zByHhlni9fep_0To130_assertion SIO_000772 21078205 NP884930.RAMIVPgIGHSNV5Np3ezwJrnfzPGV0zByHhlni9fep_0To130_provenance.
- NP884930.RAMIVPgIGHSNV5Np3ezwJrnfzPGV0zByHhlni9fep_0To130_assertion wasDerivedFrom befree-20140225 NP884930.RAMIVPgIGHSNV5Np3ezwJrnfzPGV0zByHhlni9fep_0To130_provenance.
- NP884930.RAMIVPgIGHSNV5Np3ezwJrnfzPGV0zByHhlni9fep_0To130_assertion wasGeneratedBy ECO_0000203 NP884930.RAMIVPgIGHSNV5Np3ezwJrnfzPGV0zByHhlni9fep_0To130_provenance.
- befree-20140225 importedOn "2014-02-25" NP884930.RAMIVPgIGHSNV5Np3ezwJrnfzPGV0zByHhlni9fep_0To130_provenance.