Matches in Nanopublications for { ?s ?p "[Our data suggest that ChLS is allelic to the ATR-X syndrome with its less severe phenotype being due to the presence of some XNP/ATR-X protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP853773.RATFVgrAdU6of3GP0oWirelH3oF6YpsydYRp_RJ-4tfB8130_assertion description "[Our data suggest that ChLS is allelic to the ATR-X syndrome with its less severe phenotype being due to the presence of some XNP/ATR-X protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853773.RATFVgrAdU6of3GP0oWirelH3oF6YpsydYRp_RJ-4tfB8130_provenance.
- NP374378.RAQ2XQtk_VTHK1h45mAOGmq-xMWgXq5eDrPi7yEqAt_lY130_assertion description "[Our data suggest that ChLS is allelic to the ATR-X syndrome with its less severe phenotype being due to the presence of some XNP/ATR-X protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374378.RAQ2XQtk_VTHK1h45mAOGmq-xMWgXq5eDrPi7yEqAt_lY130_provenance.
- NP608351.RAkXMswilMD5bZoNPF5vtLqXpg5r6EZK8AKBWROQTd3uI130_assertion description "[Our data suggest that ChLS is allelic to the ATR-X syndrome with its less severe phenotype being due to the presence of some XNP/ATR-X protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP608351.RAkXMswilMD5bZoNPF5vtLqXpg5r6EZK8AKBWROQTd3uI130_provenance.
- assertion description "[Our data suggest that ChLS is allelic to the ATR-X syndrome with its less severe phenotype being due to the presence of some XNP/ATR-X protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP408825.RAE-EucAPEQQFB36Vm7MvDmImAAnaZT7B9P28nTrnnXOY130_assertion description "[Our data suggest that ChLS is allelic to the ATR-X syndrome with its less severe phenotype being due to the presence of some XNP/ATR-X protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408825.RAE-EucAPEQQFB36Vm7MvDmImAAnaZT7B9P28nTrnnXOY130_provenance.
- assertion description "[Our data suggest that ChLS is allelic to the ATR-X syndrome with its less severe phenotype being due to the presence of some XNP/ATR-X protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_assertion description "[Our data suggest that ChLS is allelic to the ATR-X syndrome with its less severe phenotype being due to the presence of some XNP/ATR-X protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_provenance.
- NP955283.RAd7Soxpw3GaX8TjERLYr5bW2Ls_uG_GRP0d69fly0hkA130_assertion description "[Our data suggest that ChLS is allelic to the ATR-X syndrome with its less severe phenotype being due to the presence of some XNP/ATR-X protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP955283.RAd7Soxpw3GaX8TjERLYr5bW2Ls_uG_GRP0d69fly0hkA130_provenance.
- NP257435.RAo-_E04M_BFTmtEK3jSFknKgdQMCtV9IZY1TBw8D_g2k130_assertion description "[Our data suggest that ChLS is allelic to the ATR-X syndrome with its less severe phenotype being due to the presence of some XNP/ATR-X protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257435.RAo-_E04M_BFTmtEK3jSFknKgdQMCtV9IZY1TBw8D_g2k130_provenance.
- NP466315.RABFVRgxst3sPY7tZCN3N-2F-kASkRos9NzFsAFEKx1lI130_assertion description "[Our data suggest that ChLS is allelic to the ATR-X syndrome with its less severe phenotype being due to the presence of some XNP/ATR-X protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP466315.RABFVRgxst3sPY7tZCN3N-2F-kASkRos9NzFsAFEKx1lI130_provenance.
- NP466312.RAcpNGvHh2o4QsZbI0_zMgLNJwOqnBnIEJOW-pYWZaPDE130_assertion description "[Our data suggest that ChLS is allelic to the ATR-X syndrome with its less severe phenotype being due to the presence of some XNP/ATR-X protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP466312.RAcpNGvHh2o4QsZbI0_zMgLNJwOqnBnIEJOW-pYWZaPDE130_provenance.
- NP466314.RAtKxSzfnDE5paCe2IN7yEqv7RaHyTQbN9nwolVnLBivw130_assertion description "[Our data suggest that ChLS is allelic to the ATR-X syndrome with its less severe phenotype being due to the presence of some XNP/ATR-X protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP466314.RAtKxSzfnDE5paCe2IN7yEqv7RaHyTQbN9nwolVnLBivw130_provenance.
- NP985017.RAG_nnUsDOn7YgpRGHba7mKT261tHBruYBOzA2lhVlGGo130_assertion description "[Our data suggest that ChLS is allelic to the ATR-X syndrome with its less severe phenotype being due to the presence of some XNP/ATR-X protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP985017.RAG_nnUsDOn7YgpRGHba7mKT261tHBruYBOzA2lhVlGGo130_provenance.
- NP990766.RAyzRMuOEoWGKaexXZ_cJMQzQIhBSzWj3oeF1OqYaAAho130_assertion description "[Our data suggest that ChLS is allelic to the ATR-X syndrome with its less severe phenotype being due to the presence of some XNP/ATR-X protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990766.RAyzRMuOEoWGKaexXZ_cJMQzQIhBSzWj3oeF1OqYaAAho130_provenance.
- NP466313.RAES8nLgWB-GAzzUqhwopcNu3VPoc6Hw1_u-OUQQmkycM130_assertion description "[Our data suggest that ChLS is allelic to the ATR-X syndrome with its less severe phenotype being due to the presence of some XNP/ATR-X protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP466313.RAES8nLgWB-GAzzUqhwopcNu3VPoc6Hw1_u-OUQQmkycM130_provenance.
- NP466319.RAN-su9tZbhiou_JkW_0givt3OoknObbhspYV2XGmFeGY130_assertion description "[Our data suggest that ChLS is allelic to the ATR-X syndrome with its less severe phenotype being due to the presence of some XNP/ATR-X protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP466319.RAN-su9tZbhiou_JkW_0givt3OoknObbhspYV2XGmFeGY130_provenance.