Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP690080.RAdh9n24pFHPsLEizmu7La5KV1cKBbW-2eWdXeUBV7mSs130_assertion> ?p ?o ?g. }
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- NP690080.RAdh9n24pFHPsLEizmu7La5KV1cKBbW-2eWdXeUBV7mSs130_assertion type Assertion NP690080.RAdh9n24pFHPsLEizmu7La5KV1cKBbW-2eWdXeUBV7mSs130_head.
- NP690080.RAdh9n24pFHPsLEizmu7La5KV1cKBbW-2eWdXeUBV7mSs130_assertion wasGeneratedBy ECO_0000203 NP690080.RAdh9n24pFHPsLEizmu7La5KV1cKBbW-2eWdXeUBV7mSs130_provenance.
- NP690080.RAdh9n24pFHPsLEizmu7La5KV1cKBbW-2eWdXeUBV7mSs130_assertion wasDerivedFrom befree-20140225 NP690080.RAdh9n24pFHPsLEizmu7La5KV1cKBbW-2eWdXeUBV7mSs130_provenance.
- NP690080.RAdh9n24pFHPsLEizmu7La5KV1cKBbW-2eWdXeUBV7mSs130_assertion SIO_000772 23428682 NP690080.RAdh9n24pFHPsLEizmu7La5KV1cKBbW-2eWdXeUBV7mSs130_provenance.
- NP690080.RAdh9n24pFHPsLEizmu7La5KV1cKBbW-2eWdXeUBV7mSs130_assertion evidence source_evidence_literature NP690080.RAdh9n24pFHPsLEizmu7La5KV1cKBbW-2eWdXeUBV7mSs130_provenance.
- NP690080.RAdh9n24pFHPsLEizmu7La5KV1cKBbW-2eWdXeUBV7mSs130_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." NP690080.RAdh9n24pFHPsLEizmu7La5KV1cKBbW-2eWdXeUBV7mSs130_provenance.