Matches in Nanopublications for { ?s ?p "[Examination of published literature revealed point mutations in DIA1R are associated with X-linked mental retardation (XLMR) and DIA1R deletion is associated with syndromes with ASD-like traits and/or XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP13231.RAt4DU9o3C9FwsUODtzy-do0uEg-LWktQNzrk2EzKG3AA130_assertion description "[Examination of published literature revealed point mutations in DIA1R are associated with X-linked mental retardation (XLMR) and DIA1R deletion is associated with syndromes with ASD-like traits and/or XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP13231.RAt4DU9o3C9FwsUODtzy-do0uEg-LWktQNzrk2EzKG3AA130_provenance.
- NP13233.RATcUaxACbFTiAuYumh_toWlC1KmxyB5Rk9_GTfg3xCPI130_assertion description "[Examination of published literature revealed point mutations in DIA1R are associated with X-linked mental retardation (XLMR) and DIA1R deletion is associated with syndromes with ASD-like traits and/or XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP13233.RATcUaxACbFTiAuYumh_toWlC1KmxyB5Rk9_GTfg3xCPI130_provenance.
- assertion description "[Examination of published literature revealed point mutations in DIA1R are associated with X-linked mental retardation (XLMR) and DIA1R deletion is associated with syndromes with ASD-like traits and/or XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP263317.RAieOqYKCqP4PCsW4C-IOmd3m-JLwFVf5hmGKV9FIgcH0130_assertion description "[Examination of published literature revealed point mutations in DIA1R are associated with X-linked mental retardation (XLMR) and DIA1R deletion is associated with syndromes with ASD-like traits and/or XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263317.RAieOqYKCqP4PCsW4C-IOmd3m-JLwFVf5hmGKV9FIgcH0130_provenance.
- NP253411.RAajAsj8VcUWNxmseS8xWpVnSwu0ctDm3zKwDxw4cJ_UE130_assertion description "[Examination of published literature revealed point mutations in DIA1R are associated with X-linked mental retardation (XLMR) and DIA1R deletion is associated with syndromes with ASD-like traits and/or XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253411.RAajAsj8VcUWNxmseS8xWpVnSwu0ctDm3zKwDxw4cJ_UE130_provenance.
- NP877777.RA9FEux6i4eCv2H70phqlD4rmgRXuEXm6-ubAMuYxaQ-E130_assertion description "[Examination of published literature revealed point mutations in DIA1R are associated with X-linked mental retardation (XLMR) and DIA1R deletion is associated with syndromes with ASD-like traits and/or XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP877777.RA9FEux6i4eCv2H70phqlD4rmgRXuEXm6-ubAMuYxaQ-E130_provenance.
- NP11934.RA987zehZXK-UBOg_jLZcGce28g8CD4JbP-7TahLHUztA130_assertion description "[Examination of published literature revealed point mutations in DIA1R are associated with X-linked mental retardation (XLMR) and DIA1R deletion is associated with syndromes with ASD-like traits and/or XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP11934.RA987zehZXK-UBOg_jLZcGce28g8CD4JbP-7TahLHUztA130_provenance.
- assertion description "[Examination of published literature revealed point mutations in DIA1R are associated with X-linked mental retardation (XLMR) and DIA1R deletion is associated with syndromes with ASD-like traits and/or XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Examination of published literature revealed point mutations in DIA1R are associated with X-linked mental retardation (XLMR) and DIA1R deletion is associated with syndromes with ASD-like traits and/or XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP945505.RAm7cUuCJZYI19lX5PuXTZ_-IvewORYqBodVAhHpgM_eQ130_assertion description "[Examination of published literature revealed point mutations in DIA1R are associated with X-linked mental retardation (XLMR) and DIA1R deletion is associated with syndromes with ASD-like traits and/or XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP945505.RAm7cUuCJZYI19lX5PuXTZ_-IvewORYqBodVAhHpgM_eQ130_provenance.
- NP867500.RAhg4It7rhYJgYv1Uj9PLlAf2rurhSnUnoMsp1ERVsL28130_assertion description "[Examination of published literature revealed point mutations in DIA1R are associated with X-linked mental retardation (XLMR) and DIA1R deletion is associated with syndromes with ASD-like traits and/or XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867500.RAhg4It7rhYJgYv1Uj9PLlAf2rurhSnUnoMsp1ERVsL28130_provenance.
- NP867499.RA6X0d1hzg2_CzYV77wLG2RI7IRhyXFsyhTlb1mtzBVac130_assertion description "[Examination of published literature revealed point mutations in DIA1R are associated with X-linked mental retardation (XLMR) and DIA1R deletion is associated with syndromes with ASD-like traits and/or XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867499.RA6X0d1hzg2_CzYV77wLG2RI7IRhyXFsyhTlb1mtzBVac130_provenance.