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- NP823981.RAvPj7YZi6ntDfEsaSjne73ZSd4sDN_H2gqWrUGb5FndA130_assertion type Assertion NP823981.RAvPj7YZi6ntDfEsaSjne73ZSd4sDN_H2gqWrUGb5FndA130_head.
- NP823981.RAvPj7YZi6ntDfEsaSjne73ZSd4sDN_H2gqWrUGb5FndA130_assertion description "[Direct duplication of 8p21.3-->p23.1: a cytogenetic anomaly associated with developmental delay without consistent clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP823981.RAvPj7YZi6ntDfEsaSjne73ZSd4sDN_H2gqWrUGb5FndA130_provenance.
- NP823981.RAvPj7YZi6ntDfEsaSjne73ZSd4sDN_H2gqWrUGb5FndA130_assertion evidence source_evidence_literature NP823981.RAvPj7YZi6ntDfEsaSjne73ZSd4sDN_H2gqWrUGb5FndA130_provenance.
- NP823981.RAvPj7YZi6ntDfEsaSjne73ZSd4sDN_H2gqWrUGb5FndA130_assertion SIO_000772 11745996 NP823981.RAvPj7YZi6ntDfEsaSjne73ZSd4sDN_H2gqWrUGb5FndA130_provenance.
- NP823981.RAvPj7YZi6ntDfEsaSjne73ZSd4sDN_H2gqWrUGb5FndA130_assertion wasDerivedFrom befree-20140225 NP823981.RAvPj7YZi6ntDfEsaSjne73ZSd4sDN_H2gqWrUGb5FndA130_provenance.
- NP823981.RAvPj7YZi6ntDfEsaSjne73ZSd4sDN_H2gqWrUGb5FndA130_assertion wasGeneratedBy ECO_0000203 NP823981.RAvPj7YZi6ntDfEsaSjne73ZSd4sDN_H2gqWrUGb5FndA130_provenance.