Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP127212.RAZVr9aNOopc13sQVZBSAK_Jsjqnfxi-s3S3z9OvCOFWY130_assertion> ?p ?o ?g. }
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- NP127212.RAZVr9aNOopc13sQVZBSAK_Jsjqnfxi-s3S3z9OvCOFWY130_assertion type Assertion NP127212.RAZVr9aNOopc13sQVZBSAK_Jsjqnfxi-s3S3z9OvCOFWY130_head.
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- 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.