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- NP190393.RA6cmh2VAUH2Cr3e09UNTA8PBdF98qUSeejteoaOlq7YY130_assertion type Assertion NP190393.RA6cmh2VAUH2Cr3e09UNTA8PBdF98qUSeejteoaOlq7YY130_head.
- NP190393.RA6cmh2VAUH2Cr3e09UNTA8PBdF98qUSeejteoaOlq7YY130_assertion wasGeneratedBy ECO_0000203 NP190393.RA6cmh2VAUH2Cr3e09UNTA8PBdF98qUSeejteoaOlq7YY130_provenance.
- NP190393.RA6cmh2VAUH2Cr3e09UNTA8PBdF98qUSeejteoaOlq7YY130_assertion wasDerivedFrom lhgdn-20090331 NP190393.RA6cmh2VAUH2Cr3e09UNTA8PBdF98qUSeejteoaOlq7YY130_provenance.
- NP190393.RA6cmh2VAUH2Cr3e09UNTA8PBdF98qUSeejteoaOlq7YY130_assertion SIO_000772 18536571 NP190393.RA6cmh2VAUH2Cr3e09UNTA8PBdF98qUSeejteoaOlq7YY130_provenance.
- NP190393.RA6cmh2VAUH2Cr3e09UNTA8PBdF98qUSeejteoaOlq7YY130_assertion evidence source_evidence_literature NP190393.RA6cmh2VAUH2Cr3e09UNTA8PBdF98qUSeejteoaOlq7YY130_provenance.
- NP190393.RA6cmh2VAUH2Cr3e09UNTA8PBdF98qUSeejteoaOlq7YY130_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." NP190393.RA6cmh2VAUH2Cr3e09UNTA8PBdF98qUSeejteoaOlq7YY130_provenance.