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- NP530584.RAARoV05LOhguXCFbD-0YKNlwn-MT-NdDl29VSq5CLHPc130_assertion type Assertion NP530584.RAARoV05LOhguXCFbD-0YKNlwn-MT-NdDl29VSq5CLHPc130_head.
- NP530584.RAARoV05LOhguXCFbD-0YKNlwn-MT-NdDl29VSq5CLHPc130_assertion wasGeneratedBy ECO_0000203 NP530584.RAARoV05LOhguXCFbD-0YKNlwn-MT-NdDl29VSq5CLHPc130_provenance.
- NP530584.RAARoV05LOhguXCFbD-0YKNlwn-MT-NdDl29VSq5CLHPc130_assertion wasDerivedFrom befree-20150227 NP530584.RAARoV05LOhguXCFbD-0YKNlwn-MT-NdDl29VSq5CLHPc130_provenance.
- NP530584.RAARoV05LOhguXCFbD-0YKNlwn-MT-NdDl29VSq5CLHPc130_assertion SIO_000772 21236492 NP530584.RAARoV05LOhguXCFbD-0YKNlwn-MT-NdDl29VSq5CLHPc130_provenance.
- NP530584.RAARoV05LOhguXCFbD-0YKNlwn-MT-NdDl29VSq5CLHPc130_assertion evidence source_evidence_literature NP530584.RAARoV05LOhguXCFbD-0YKNlwn-MT-NdDl29VSq5CLHPc130_provenance.
- NP530584.RAARoV05LOhguXCFbD-0YKNlwn-MT-NdDl29VSq5CLHPc130_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." NP530584.RAARoV05LOhguXCFbD-0YKNlwn-MT-NdDl29VSq5CLHPc130_provenance.