Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP127212.RAZVr9aNOopc13sQVZBSAK_Jsjqnfxi-s3S3z9OvCOFWY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP127212.RAZVr9aNOopc13sQVZBSAK_Jsjqnfxi-s3S3z9OvCOFWY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP127212.RAZVr9aNOopc13sQVZBSAK_Jsjqnfxi-s3S3z9OvCOFWY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP127212.RAZVr9aNOopc13sQVZBSAK_Jsjqnfxi-s3S3z9OvCOFWY130_provenance.
- NP127212.RAZVr9aNOopc13sQVZBSAK_Jsjqnfxi-s3S3z9OvCOFWY130_assertion wasGeneratedBy ECO_0000203 NP127212.RAZVr9aNOopc13sQVZBSAK_Jsjqnfxi-s3S3z9OvCOFWY130_provenance.
- NP127212.RAZVr9aNOopc13sQVZBSAK_Jsjqnfxi-s3S3z9OvCOFWY130_assertion wasDerivedFrom lhgdn-20090331 NP127212.RAZVr9aNOopc13sQVZBSAK_Jsjqnfxi-s3S3z9OvCOFWY130_provenance.
- NP127212.RAZVr9aNOopc13sQVZBSAK_Jsjqnfxi-s3S3z9OvCOFWY130_assertion SIO_000772 18536571 NP127212.RAZVr9aNOopc13sQVZBSAK_Jsjqnfxi-s3S3z9OvCOFWY130_provenance.
- NP127212.RAZVr9aNOopc13sQVZBSAK_Jsjqnfxi-s3S3z9OvCOFWY130_assertion evidence source_evidence_literature NP127212.RAZVr9aNOopc13sQVZBSAK_Jsjqnfxi-s3S3z9OvCOFWY130_provenance.
- NP127212.RAZVr9aNOopc13sQVZBSAK_Jsjqnfxi-s3S3z9OvCOFWY130_assertion description "[REVIEW: Congenital neutropenia patients with acquired CSF3R mutations define a group with high risk for development of leukemia; discussion of possible pathomechanism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP127212.RAZVr9aNOopc13sQVZBSAK_Jsjqnfxi-s3S3z9OvCOFWY130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP127212.RAZVr9aNOopc13sQVZBSAK_Jsjqnfxi-s3S3z9OvCOFWY130_provenance.