Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP910852.RAniXxU4LDYNl4IOg4vY2ekiBQU5Of03IQmM23SSdVX6U130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP910852.RAniXxU4LDYNl4IOg4vY2ekiBQU5Of03IQmM23SSdVX6U130_assertion type Assertion NP910852.RAniXxU4LDYNl4IOg4vY2ekiBQU5Of03IQmM23SSdVX6U130_head.
- 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.
- NP910852.RAniXxU4LDYNl4IOg4vY2ekiBQU5Of03IQmM23SSdVX6U130_assertion evidence source_evidence_literature NP910852.RAniXxU4LDYNl4IOg4vY2ekiBQU5Of03IQmM23SSdVX6U130_provenance.
- NP910852.RAniXxU4LDYNl4IOg4vY2ekiBQU5Of03IQmM23SSdVX6U130_assertion SIO_000772 21569590 NP910852.RAniXxU4LDYNl4IOg4vY2ekiBQU5Of03IQmM23SSdVX6U130_provenance.
- NP910852.RAniXxU4LDYNl4IOg4vY2ekiBQU5Of03IQmM23SSdVX6U130_assertion wasDerivedFrom befree-20150227 NP910852.RAniXxU4LDYNl4IOg4vY2ekiBQU5Of03IQmM23SSdVX6U130_provenance.
- NP910852.RAniXxU4LDYNl4IOg4vY2ekiBQU5Of03IQmM23SSdVX6U130_assertion wasGeneratedBy ECO_0000203 NP910852.RAniXxU4LDYNl4IOg4vY2ekiBQU5Of03IQmM23SSdVX6U130_provenance.