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- NP607091.RAL1BQNBlwbfLBYEKRIjN5Qn-kd6tQ8Op7vHgVW5CsIQ8130_assertion type Assertion NP607091.RAL1BQNBlwbfLBYEKRIjN5Qn-kd6tQ8Op7vHgVW5CsIQ8130_head.
- NP607091.RAL1BQNBlwbfLBYEKRIjN5Qn-kd6tQ8Op7vHgVW5CsIQ8130_assertion wasGeneratedBy ECO_0000203 NP607091.RAL1BQNBlwbfLBYEKRIjN5Qn-kd6tQ8Op7vHgVW5CsIQ8130_provenance.
- NP607091.RAL1BQNBlwbfLBYEKRIjN5Qn-kd6tQ8Op7vHgVW5CsIQ8130_assertion wasDerivedFrom befree-2016 NP607091.RAL1BQNBlwbfLBYEKRIjN5Qn-kd6tQ8Op7vHgVW5CsIQ8130_provenance.
- NP607091.RAL1BQNBlwbfLBYEKRIjN5Qn-kd6tQ8Op7vHgVW5CsIQ8130_assertion SIO_000772 17466001 NP607091.RAL1BQNBlwbfLBYEKRIjN5Qn-kd6tQ8Op7vHgVW5CsIQ8130_provenance.
- NP607091.RAL1BQNBlwbfLBYEKRIjN5Qn-kd6tQ8Op7vHgVW5CsIQ8130_assertion evidence source_evidence_literature NP607091.RAL1BQNBlwbfLBYEKRIjN5Qn-kd6tQ8Op7vHgVW5CsIQ8130_provenance.
- NP607091.RAL1BQNBlwbfLBYEKRIjN5Qn-kd6tQ8Op7vHgVW5CsIQ8130_assertion description "[Patients lacked mutations in other genes known to cause ACTH resistance, including AAAS for patients diagnosed with triple A syndrome and MC2R and MRAP for patients diagnosed with familial glucocorticoid deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP607091.RAL1BQNBlwbfLBYEKRIjN5Qn-kd6tQ8Op7vHgVW5CsIQ8130_provenance.