Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP527127.RADFpBu38gL-8lHaAcViTgLgtvrR4xItl6Ov9QBLIpqIk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP527127.RADFpBu38gL-8lHaAcViTgLgtvrR4xItl6Ov9QBLIpqIk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP527127.RADFpBu38gL-8lHaAcViTgLgtvrR4xItl6Ov9QBLIpqIk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP527127.RADFpBu38gL-8lHaAcViTgLgtvrR4xItl6Ov9QBLIpqIk130_provenance.
- NP527127.RADFpBu38gL-8lHaAcViTgLgtvrR4xItl6Ov9QBLIpqIk130_assertion description "[Results showed that the difference between the frequencies of DRB1*13 in patients and normal individuals was significant (p=0.04), but there was a moderate difference among the frequencies of DRB1*04, *07, and *09 in childhood (0-15 years) ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP527127.RADFpBu38gL-8lHaAcViTgLgtvrR4xItl6Ov9QBLIpqIk130_provenance.
- NP527127.RADFpBu38gL-8lHaAcViTgLgtvrR4xItl6Ov9QBLIpqIk130_assertion evidence source_evidence_literature NP527127.RADFpBu38gL-8lHaAcViTgLgtvrR4xItl6Ov9QBLIpqIk130_provenance.
- NP527127.RADFpBu38gL-8lHaAcViTgLgtvrR4xItl6Ov9QBLIpqIk130_assertion SIO_000772 18164964 NP527127.RADFpBu38gL-8lHaAcViTgLgtvrR4xItl6Ov9QBLIpqIk130_provenance.
- NP527127.RADFpBu38gL-8lHaAcViTgLgtvrR4xItl6Ov9QBLIpqIk130_assertion wasDerivedFrom befree-20140225 NP527127.RADFpBu38gL-8lHaAcViTgLgtvrR4xItl6Ov9QBLIpqIk130_provenance.
- NP527127.RADFpBu38gL-8lHaAcViTgLgtvrR4xItl6Ov9QBLIpqIk130_assertion wasGeneratedBy ECO_0000203 NP527127.RADFpBu38gL-8lHaAcViTgLgtvrR4xItl6Ov9QBLIpqIk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP527127.RADFpBu38gL-8lHaAcViTgLgtvrR4xItl6Ov9QBLIpqIk130_provenance.