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- NP341792.RAEnYTs2eUsF9h6JBe00ZAMxOpNl_yaJEzzdhSTkuAnrc130_assertion type Assertion NP341792.RAEnYTs2eUsF9h6JBe00ZAMxOpNl_yaJEzzdhSTkuAnrc130_head.
- NP341792.RAEnYTs2eUsF9h6JBe00ZAMxOpNl_yaJEzzdhSTkuAnrc130_assertion wasGeneratedBy ECO_0000203 NP341792.RAEnYTs2eUsF9h6JBe00ZAMxOpNl_yaJEzzdhSTkuAnrc130_provenance.
- NP341792.RAEnYTs2eUsF9h6JBe00ZAMxOpNl_yaJEzzdhSTkuAnrc130_assertion wasDerivedFrom befree-20140225 NP341792.RAEnYTs2eUsF9h6JBe00ZAMxOpNl_yaJEzzdhSTkuAnrc130_provenance.
- NP341792.RAEnYTs2eUsF9h6JBe00ZAMxOpNl_yaJEzzdhSTkuAnrc130_assertion SIO_000772 21236492 NP341792.RAEnYTs2eUsF9h6JBe00ZAMxOpNl_yaJEzzdhSTkuAnrc130_provenance.
- NP341792.RAEnYTs2eUsF9h6JBe00ZAMxOpNl_yaJEzzdhSTkuAnrc130_assertion evidence source_evidence_literature NP341792.RAEnYTs2eUsF9h6JBe00ZAMxOpNl_yaJEzzdhSTkuAnrc130_provenance.
- NP341792.RAEnYTs2eUsF9h6JBe00ZAMxOpNl_yaJEzzdhSTkuAnrc130_assertion description "[A novel mutation of LAMB2 in a multigenerational mennonite family reveals a new phenotypic variant of Pierson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP341792.RAEnYTs2eUsF9h6JBe00ZAMxOpNl_yaJEzzdhSTkuAnrc130_provenance.