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- NP306470.RAkgjIKwetKgH5-t_w7TE3d9Zz0ZYfLrc4aJ_AD_pl6ok130_assertion type Assertion NP306470.RAkgjIKwetKgH5-t_w7TE3d9Zz0ZYfLrc4aJ_AD_pl6ok130_head.
- NP306470.RAkgjIKwetKgH5-t_w7TE3d9Zz0ZYfLrc4aJ_AD_pl6ok130_assertion wasGeneratedBy ECO_0000203 NP306470.RAkgjIKwetKgH5-t_w7TE3d9Zz0ZYfLrc4aJ_AD_pl6ok130_provenance.
- NP306470.RAkgjIKwetKgH5-t_w7TE3d9Zz0ZYfLrc4aJ_AD_pl6ok130_assertion wasDerivedFrom befree-20140225 NP306470.RAkgjIKwetKgH5-t_w7TE3d9Zz0ZYfLrc4aJ_AD_pl6ok130_provenance.
- NP306470.RAkgjIKwetKgH5-t_w7TE3d9Zz0ZYfLrc4aJ_AD_pl6ok130_assertion SIO_000772 11749051 NP306470.RAkgjIKwetKgH5-t_w7TE3d9Zz0ZYfLrc4aJ_AD_pl6ok130_provenance.
- NP306470.RAkgjIKwetKgH5-t_w7TE3d9Zz0ZYfLrc4aJ_AD_pl6ok130_assertion evidence source_evidence_literature NP306470.RAkgjIKwetKgH5-t_w7TE3d9Zz0ZYfLrc4aJ_AD_pl6ok130_provenance.
- NP306470.RAkgjIKwetKgH5-t_w7TE3d9Zz0ZYfLrc4aJ_AD_pl6ok130_assertion description "[Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP306470.RAkgjIKwetKgH5-t_w7TE3d9Zz0ZYfLrc4aJ_AD_pl6ok130_provenance.