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- NP4877.RA-ecgPgzNE19H_TvAv9kLWHCeJkklH-BJMoGJ2HRO704130_assertion type Assertion NP4877.RA-ecgPgzNE19H_TvAv9kLWHCeJkklH-BJMoGJ2HRO704130_head.
- NP4877.RA-ecgPgzNE19H_TvAv9kLWHCeJkklH-BJMoGJ2HRO704130_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." NP4877.RA-ecgPgzNE19H_TvAv9kLWHCeJkklH-BJMoGJ2HRO704130_provenance.
- NP4877.RA-ecgPgzNE19H_TvAv9kLWHCeJkklH-BJMoGJ2HRO704130_assertion evidence source_evidence_curated NP4877.RA-ecgPgzNE19H_TvAv9kLWHCeJkklH-BJMoGJ2HRO704130_provenance.
- NP4877.RA-ecgPgzNE19H_TvAv9kLWHCeJkklH-BJMoGJ2HRO704130_assertion SIO_000772 18523010 NP4877.RA-ecgPgzNE19H_TvAv9kLWHCeJkklH-BJMoGJ2HRO704130_provenance.
- NP4877.RA-ecgPgzNE19H_TvAv9kLWHCeJkklH-BJMoGJ2HRO704130_assertion wasDerivedFrom uniprot-20150221 NP4877.RA-ecgPgzNE19H_TvAv9kLWHCeJkklH-BJMoGJ2HRO704130_provenance.
- NP4877.RA-ecgPgzNE19H_TvAv9kLWHCeJkklH-BJMoGJ2HRO704130_assertion wasGeneratedBy ECO_0000218 NP4877.RA-ecgPgzNE19H_TvAv9kLWHCeJkklH-BJMoGJ2HRO704130_provenance.