Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP893956.RAJ48As1_1JLxkSg_GeSie4wQel9qX2Uh7kWvpLR5TeKY130_assertion> ?p ?o ?g. }
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- NP893956.RAJ48As1_1JLxkSg_GeSie4wQel9qX2Uh7kWvpLR5TeKY130_assertion type Assertion NP893956.RAJ48As1_1JLxkSg_GeSie4wQel9qX2Uh7kWvpLR5TeKY130_head.
- 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.
- NP893956.RAJ48As1_1JLxkSg_GeSie4wQel9qX2Uh7kWvpLR5TeKY130_assertion evidence source_evidence_literature NP893956.RAJ48As1_1JLxkSg_GeSie4wQel9qX2Uh7kWvpLR5TeKY130_provenance.
- NP893956.RAJ48As1_1JLxkSg_GeSie4wQel9qX2Uh7kWvpLR5TeKY130_assertion SIO_000772 21569590 NP893956.RAJ48As1_1JLxkSg_GeSie4wQel9qX2Uh7kWvpLR5TeKY130_provenance.
- NP893956.RAJ48As1_1JLxkSg_GeSie4wQel9qX2Uh7kWvpLR5TeKY130_assertion wasDerivedFrom befree-2016 NP893956.RAJ48As1_1JLxkSg_GeSie4wQel9qX2Uh7kWvpLR5TeKY130_provenance.
- NP893956.RAJ48As1_1JLxkSg_GeSie4wQel9qX2Uh7kWvpLR5TeKY130_assertion wasGeneratedBy ECO_0000203 NP893956.RAJ48As1_1JLxkSg_GeSie4wQel9qX2Uh7kWvpLR5TeKY130_provenance.