Matches in Nanopublications for { ?s ?p "[A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP910852.RAniXxU4LDYNl4IOg4vY2ekiBQU5Of03IQmM23SSdVX6U130_assertion description "[A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP910852.RAniXxU4LDYNl4IOg4vY2ekiBQU5Of03IQmM23SSdVX6U130_provenance.
- NP893955.RAPOqzE0QXct8N2ChMxmCq5Qp4XVAlwIt25ynk0Lhll5s130_assertion description "[A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP893955.RAPOqzE0QXct8N2ChMxmCq5Qp4XVAlwIt25ynk0Lhll5s130_provenance.
- NP893956.RAJ48As1_1JLxkSg_GeSie4wQel9qX2Uh7kWvpLR5TeKY130_assertion description "[A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP893956.RAJ48As1_1JLxkSg_GeSie4wQel9qX2Uh7kWvpLR5TeKY130_provenance.
- NP930750.RA4n6h5AZenjLszH6DoiGC_Jm_Y7ZX_ZNmsLNsruVpJuE130_assertion description "[A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP930750.RA4n6h5AZenjLszH6DoiGC_Jm_Y7ZX_ZNmsLNsruVpJuE130_provenance.