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- NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_assertion type Assertion NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_head.
- NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_assertion description "[In summary, although heterozygous loss-of- function mutations in AKT2 can cause a syndrome of severe insulin resistance and lipodystrophy in humans, such mutations are uncommon causes of these syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_provenance.
- NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_assertion evidence source_evidence_literature NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_provenance.
- NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_assertion SIO_000772 17327441 NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_provenance.
- NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_assertion wasDerivedFrom befree-20150227 NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_provenance.
- NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_assertion wasGeneratedBy ECO_0000203 NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_provenance.