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- NP674838.RA0cp3QtpV7aqb--70-Nk4_EJjsuBUHjlFqg0bisfXZFg130_assertion type Assertion NP674838.RA0cp3QtpV7aqb--70-Nk4_EJjsuBUHjlFqg0bisfXZFg130_head.
- NP674838.RA0cp3QtpV7aqb--70-Nk4_EJjsuBUHjlFqg0bisfXZFg130_assertion description "[Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674838.RA0cp3QtpV7aqb--70-Nk4_EJjsuBUHjlFqg0bisfXZFg130_provenance.
- NP674838.RA0cp3QtpV7aqb--70-Nk4_EJjsuBUHjlFqg0bisfXZFg130_assertion evidence source_evidence_literature NP674838.RA0cp3QtpV7aqb--70-Nk4_EJjsuBUHjlFqg0bisfXZFg130_provenance.
- NP674838.RA0cp3QtpV7aqb--70-Nk4_EJjsuBUHjlFqg0bisfXZFg130_assertion SIO_000772 18523010 NP674838.RA0cp3QtpV7aqb--70-Nk4_EJjsuBUHjlFqg0bisfXZFg130_provenance.
- NP674838.RA0cp3QtpV7aqb--70-Nk4_EJjsuBUHjlFqg0bisfXZFg130_assertion wasDerivedFrom befree-2016 NP674838.RA0cp3QtpV7aqb--70-Nk4_EJjsuBUHjlFqg0bisfXZFg130_provenance.
- NP674838.RA0cp3QtpV7aqb--70-Nk4_EJjsuBUHjlFqg0bisfXZFg130_assertion wasGeneratedBy ECO_0000203 NP674838.RA0cp3QtpV7aqb--70-Nk4_EJjsuBUHjlFqg0bisfXZFg130_provenance.