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- NP482697.RAEo8V0L4VuMQrXpROSuYjtJAq1YGl-JYnEx1m6XI4IuQ130_assertion type Assertion NP482697.RAEo8V0L4VuMQrXpROSuYjtJAq1YGl-JYnEx1m6XI4IuQ130_head.
- NP482697.RAEo8V0L4VuMQrXpROSuYjtJAq1YGl-JYnEx1m6XI4IuQ130_assertion wasGeneratedBy ECO_0000203 NP482697.RAEo8V0L4VuMQrXpROSuYjtJAq1YGl-JYnEx1m6XI4IuQ130_provenance.
- NP482697.RAEo8V0L4VuMQrXpROSuYjtJAq1YGl-JYnEx1m6XI4IuQ130_assertion wasDerivedFrom befree-20150227 NP482697.RAEo8V0L4VuMQrXpROSuYjtJAq1YGl-JYnEx1m6XI4IuQ130_provenance.
- NP482697.RAEo8V0L4VuMQrXpROSuYjtJAq1YGl-JYnEx1m6XI4IuQ130_assertion SIO_000772 23428682 NP482697.RAEo8V0L4VuMQrXpROSuYjtJAq1YGl-JYnEx1m6XI4IuQ130_provenance.
- NP482697.RAEo8V0L4VuMQrXpROSuYjtJAq1YGl-JYnEx1m6XI4IuQ130_assertion evidence source_evidence_literature NP482697.RAEo8V0L4VuMQrXpROSuYjtJAq1YGl-JYnEx1m6XI4IuQ130_provenance.
- NP482697.RAEo8V0L4VuMQrXpROSuYjtJAq1YGl-JYnEx1m6XI4IuQ130_assertion description "[Patients with heterozygous mutations or deletions of IGF1R have a moderate pre- and postnatal growth failure, microcephaly and a history of feeding problems.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP482697.RAEo8V0L4VuMQrXpROSuYjtJAq1YGl-JYnEx1m6XI4IuQ130_provenance.