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- NP136854.RAYN6j8bM_mqrC237ITM-Je8ZlqJebiB-L-TTWMNx7cCY130_assertion type Assertion NP136854.RAYN6j8bM_mqrC237ITM-Je8ZlqJebiB-L-TTWMNx7cCY130_head.
- NP136854.RAYN6j8bM_mqrC237ITM-Je8ZlqJebiB-L-TTWMNx7cCY130_assertion wasGeneratedBy ECO_0000203 NP136854.RAYN6j8bM_mqrC237ITM-Je8ZlqJebiB-L-TTWMNx7cCY130_provenance.
- NP136854.RAYN6j8bM_mqrC237ITM-Je8ZlqJebiB-L-TTWMNx7cCY130_assertion wasDerivedFrom lhgdn-20090331 NP136854.RAYN6j8bM_mqrC237ITM-Je8ZlqJebiB-L-TTWMNx7cCY130_provenance.
- NP136854.RAYN6j8bM_mqrC237ITM-Je8ZlqJebiB-L-TTWMNx7cCY130_assertion SIO_000772 18989701 NP136854.RAYN6j8bM_mqrC237ITM-Je8ZlqJebiB-L-TTWMNx7cCY130_provenance.
- NP136854.RAYN6j8bM_mqrC237ITM-Je8ZlqJebiB-L-TTWMNx7cCY130_assertion evidence source_evidence_literature NP136854.RAYN6j8bM_mqrC237ITM-Je8ZlqJebiB-L-TTWMNx7cCY130_provenance.
- NP136854.RAYN6j8bM_mqrC237ITM-Je8ZlqJebiB-L-TTWMNx7cCY130_assertion description "[a gradient of impairment is present when the p.P152A mutation is compared with an allelic p.P152R mutation, which causes classic Rett syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136854.RAYN6j8bM_mqrC237ITM-Je8ZlqJebiB-L-TTWMNx7cCY130_provenance.