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- NP948084.RADWzF-kE9cclsV_1mw0X6P8gj2_UHfV_sfl2Gv5Yxsos130_assertion type Assertion NP948084.RADWzF-kE9cclsV_1mw0X6P8gj2_UHfV_sfl2Gv5Yxsos130_head.
- NP948084.RADWzF-kE9cclsV_1mw0X6P8gj2_UHfV_sfl2Gv5Yxsos130_assertion wasGeneratedBy ECO_0000203 NP948084.RADWzF-kE9cclsV_1mw0X6P8gj2_UHfV_sfl2Gv5Yxsos130_provenance.
- NP948084.RADWzF-kE9cclsV_1mw0X6P8gj2_UHfV_sfl2Gv5Yxsos130_assertion wasDerivedFrom befree-20150227 NP948084.RADWzF-kE9cclsV_1mw0X6P8gj2_UHfV_sfl2Gv5Yxsos130_provenance.
- NP948084.RADWzF-kE9cclsV_1mw0X6P8gj2_UHfV_sfl2Gv5Yxsos130_assertion SIO_000772 24115768 NP948084.RADWzF-kE9cclsV_1mw0X6P8gj2_UHfV_sfl2Gv5Yxsos130_provenance.
- NP948084.RADWzF-kE9cclsV_1mw0X6P8gj2_UHfV_sfl2Gv5Yxsos130_assertion evidence source_evidence_literature NP948084.RADWzF-kE9cclsV_1mw0X6P8gj2_UHfV_sfl2Gv5Yxsos130_provenance.
- NP948084.RADWzF-kE9cclsV_1mw0X6P8gj2_UHfV_sfl2Gv5Yxsos130_assertion description "[Mutations in CTC1 lead to the telomere syndromes Coats Plus and dyskeratosis congenita (DC), but the molecular mechanisms involved remain unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948084.RADWzF-kE9cclsV_1mw0X6P8gj2_UHfV_sfl2Gv5Yxsos130_provenance.