Matches in Nanopublications for { ?s ?p "[The occurrence of epilepsy with mental retardation limited to females (EFMR; MIM 300088) has been recently associated to mutations in the PCDH19 gene, located on chromosome X and encoding for protocadherin 19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP626291.RArUxO8nuPn47G119A8rF-4twhE1YMwrrv--IEmdvzkdA130_assertion description "[The occurrence of epilepsy with mental retardation limited to females (EFMR; MIM 300088) has been recently associated to mutations in the PCDH19 gene, located on chromosome X and encoding for protocadherin 19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626291.RArUxO8nuPn47G119A8rF-4twhE1YMwrrv--IEmdvzkdA130_provenance.
- NP210674.RAnB2kp7MrINyX1UGxpcAPVMSDn3XROJp64qRoyVC9yFU130_assertion description "[The occurrence of epilepsy with mental retardation limited to females (EFMR; MIM 300088) has been recently associated to mutations in the PCDH19 gene, located on chromosome X and encoding for protocadherin 19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210674.RAnB2kp7MrINyX1UGxpcAPVMSDn3XROJp64qRoyVC9yFU130_provenance.
- NP839443.RApMU6j-rZE63HHsfGmgBbfhSdrb-zGbU0caJ75DP7400130_assertion description "[The occurrence of epilepsy with mental retardation limited to females (EFMR; MIM 300088) has been recently associated to mutations in the PCDH19 gene, located on chromosome X and encoding for protocadherin 19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP839443.RApMU6j-rZE63HHsfGmgBbfhSdrb-zGbU0caJ75DP7400130_provenance.
- assertion description "[The occurrence of epilepsy with mental retardation limited to females (EFMR; MIM 300088) has been recently associated to mutations in the PCDH19 gene, located on chromosome X and encoding for protocadherin 19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The occurrence of epilepsy with mental retardation limited to females (EFMR; MIM 300088) has been recently associated to mutations in the PCDH19 gene, located on chromosome X and encoding for protocadherin 19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The occurrence of epilepsy with mental retardation limited to females (EFMR; MIM 300088) has been recently associated to mutations in the PCDH19 gene, located on chromosome X and encoding for protocadherin 19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1010346.RAazzg0fU5Vg6if9qIuFnU3KQCfMf6ERPsQncInc9wLp0130_assertion description "[The occurrence of epilepsy with mental retardation limited to females (EFMR; MIM 300088) has been recently associated to mutations in the PCDH19 gene, located on chromosome X and encoding for protocadherin 19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1010346.RAazzg0fU5Vg6if9qIuFnU3KQCfMf6ERPsQncInc9wLp0130_provenance.
- NP931108.RAp9__0wBhK701OBzj8ofDqJmA2OvDaUs0aiIoULtjcoI130_assertion description "[The occurrence of epilepsy with mental retardation limited to females (EFMR; MIM 300088) has been recently associated to mutations in the PCDH19 gene, located on chromosome X and encoding for protocadherin 19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP931108.RAp9__0wBhK701OBzj8ofDqJmA2OvDaUs0aiIoULtjcoI130_provenance.
- NP932052.RAjnsH1my71Rmr5ROUfLc6e2igakvpSzro7ehayHJHcj8130_assertion description "[The occurrence of epilepsy with mental retardation limited to females (EFMR; MIM 300088) has been recently associated to mutations in the PCDH19 gene, located on chromosome X and encoding for protocadherin 19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932052.RAjnsH1my71Rmr5ROUfLc6e2igakvpSzro7ehayHJHcj8130_provenance.
- NP1010343.RAIdhY5HZGJq2XBEFgm1Y7ufhW73FFH16XRmOboF8rkXc130_assertion description "[The occurrence of epilepsy with mental retardation limited to females (EFMR; MIM 300088) has been recently associated to mutations in the PCDH19 gene, located on chromosome X and encoding for protocadherin 19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1010343.RAIdhY5HZGJq2XBEFgm1Y7ufhW73FFH16XRmOboF8rkXc130_provenance.
- NP1010344.RAK0MBkz7VZOXnHHHfzAgDoC5DqtRYzZnh5aeO5jfuhdQ130_assertion description "[The occurrence of epilepsy with mental retardation limited to females (EFMR; MIM 300088) has been recently associated to mutations in the PCDH19 gene, located on chromosome X and encoding for protocadherin 19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1010344.RAK0MBkz7VZOXnHHHfzAgDoC5DqtRYzZnh5aeO5jfuhdQ130_provenance.
- NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_assertion description "[The occurrence of epilepsy with mental retardation limited to females (EFMR; MIM 300088) has been recently associated to mutations in the PCDH19 gene, located on chromosome X and encoding for protocadherin 19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1010345.RA0CtBGVyjvzTEgi4HdFbUBWfBkTAcptcvN6hSowqImAQ130_provenance.
- NP932076.RA0vMNR2__nkJmxuxkKZ5YxszL4gByWZ17-cS5PYw1iMU130_assertion description "[The occurrence of epilepsy with mental retardation limited to females (EFMR; MIM 300088) has been recently associated to mutations in the PCDH19 gene, located on chromosome X and encoding for protocadherin 19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932076.RA0vMNR2__nkJmxuxkKZ5YxszL4gByWZ17-cS5PYw1iMU130_provenance.