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- NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_assertion type Assertion NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_head.
- NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_assertion description "[HGPS (Hutchinson-Gilford progeria syndrome) is a rare genetic disease affecting children causing them to age and die prematurely.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_provenance.
- NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_assertion evidence source_evidence_literature NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_provenance.
- NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_assertion SIO_000772 20074076 NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_provenance.
- NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_assertion wasDerivedFrom befree-20150227 NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_provenance.
- NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_assertion wasGeneratedBy ECO_0000203 NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_provenance.