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- NP330748.RAivyo8ukon2aaEUtMRQn49nlKf9iTCalx5_adPROwU3o130_assertion type Assertion NP330748.RAivyo8ukon2aaEUtMRQn49nlKf9iTCalx5_adPROwU3o130_head.
- NP330748.RAivyo8ukon2aaEUtMRQn49nlKf9iTCalx5_adPROwU3o130_assertion description "[Genetic mutations that disrupt GM-CSF receptor signaling comprise a rare form of hereditary PAP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330748.RAivyo8ukon2aaEUtMRQn49nlKf9iTCalx5_adPROwU3o130_provenance.
- NP330748.RAivyo8ukon2aaEUtMRQn49nlKf9iTCalx5_adPROwU3o130_assertion evidence source_evidence_literature NP330748.RAivyo8ukon2aaEUtMRQn49nlKf9iTCalx5_adPROwU3o130_provenance.
- NP330748.RAivyo8ukon2aaEUtMRQn49nlKf9iTCalx5_adPROwU3o130_assertion SIO_000772 20338813 NP330748.RAivyo8ukon2aaEUtMRQn49nlKf9iTCalx5_adPROwU3o130_provenance.
- NP330748.RAivyo8ukon2aaEUtMRQn49nlKf9iTCalx5_adPROwU3o130_assertion wasDerivedFrom befree-20150227 NP330748.RAivyo8ukon2aaEUtMRQn49nlKf9iTCalx5_adPROwU3o130_provenance.
- NP330748.RAivyo8ukon2aaEUtMRQn49nlKf9iTCalx5_adPROwU3o130_assertion wasGeneratedBy ECO_0000203 NP330748.RAivyo8ukon2aaEUtMRQn49nlKf9iTCalx5_adPROwU3o130_provenance.