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- NP915778.RAkn4_2n7Wn-rhP8HOSI4c0YQZO3DqmI7K7MqBfI66rk0130_assertion type Assertion NP915778.RAkn4_2n7Wn-rhP8HOSI4c0YQZO3DqmI7K7MqBfI66rk0130_head.
- NP915778.RAkn4_2n7Wn-rhP8HOSI4c0YQZO3DqmI7K7MqBfI66rk0130_assertion description "[Mutations in the human ATGL gene are associated with neutral lipid storage disease with myopathy, a rare genetic disease characterized by excessive accumulation of TG in multiple tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915778.RAkn4_2n7Wn-rhP8HOSI4c0YQZO3DqmI7K7MqBfI66rk0130_provenance.
- NP915778.RAkn4_2n7Wn-rhP8HOSI4c0YQZO3DqmI7K7MqBfI66rk0130_assertion evidence source_evidence_literature NP915778.RAkn4_2n7Wn-rhP8HOSI4c0YQZO3DqmI7K7MqBfI66rk0130_provenance.
- NP915778.RAkn4_2n7Wn-rhP8HOSI4c0YQZO3DqmI7K7MqBfI66rk0130_assertion SIO_000772 21828047 NP915778.RAkn4_2n7Wn-rhP8HOSI4c0YQZO3DqmI7K7MqBfI66rk0130_provenance.
- NP915778.RAkn4_2n7Wn-rhP8HOSI4c0YQZO3DqmI7K7MqBfI66rk0130_assertion wasDerivedFrom befree-2016 NP915778.RAkn4_2n7Wn-rhP8HOSI4c0YQZO3DqmI7K7MqBfI66rk0130_provenance.
- NP915778.RAkn4_2n7Wn-rhP8HOSI4c0YQZO3DqmI7K7MqBfI66rk0130_assertion wasGeneratedBy ECO_0000203 NP915778.RAkn4_2n7Wn-rhP8HOSI4c0YQZO3DqmI7K7MqBfI66rk0130_provenance.