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- NP822670.RAJ-mS_y26D3ae0HX0gBJYm6AzDuptCWPfejgPG9ZptbQ130_assertion type Assertion NP822670.RAJ-mS_y26D3ae0HX0gBJYm6AzDuptCWPfejgPG9ZptbQ130_head.
- NP822670.RAJ-mS_y26D3ae0HX0gBJYm6AzDuptCWPfejgPG9ZptbQ130_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." NP822670.RAJ-mS_y26D3ae0HX0gBJYm6AzDuptCWPfejgPG9ZptbQ130_provenance.
- NP822670.RAJ-mS_y26D3ae0HX0gBJYm6AzDuptCWPfejgPG9ZptbQ130_assertion evidence source_evidence_literature NP822670.RAJ-mS_y26D3ae0HX0gBJYm6AzDuptCWPfejgPG9ZptbQ130_provenance.
- NP822670.RAJ-mS_y26D3ae0HX0gBJYm6AzDuptCWPfejgPG9ZptbQ130_assertion SIO_000772 11745996 NP822670.RAJ-mS_y26D3ae0HX0gBJYm6AzDuptCWPfejgPG9ZptbQ130_provenance.
- NP822670.RAJ-mS_y26D3ae0HX0gBJYm6AzDuptCWPfejgPG9ZptbQ130_assertion wasDerivedFrom befree-20140225 NP822670.RAJ-mS_y26D3ae0HX0gBJYm6AzDuptCWPfejgPG9ZptbQ130_provenance.
- NP822670.RAJ-mS_y26D3ae0HX0gBJYm6AzDuptCWPfejgPG9ZptbQ130_assertion wasGeneratedBy ECO_0000203 NP822670.RAJ-mS_y26D3ae0HX0gBJYm6AzDuptCWPfejgPG9ZptbQ130_provenance.