Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP699592.RAaXeazEtGqMZbnvyPntT2rRiCYUDhiAKIegSkksyW9vk130_assertion> ?p ?o ?g. }
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- NP699592.RAaXeazEtGqMZbnvyPntT2rRiCYUDhiAKIegSkksyW9vk130_assertion type Assertion NP699592.RAaXeazEtGqMZbnvyPntT2rRiCYUDhiAKIegSkksyW9vk130_head.
- NP699592.RAaXeazEtGqMZbnvyPntT2rRiCYUDhiAKIegSkksyW9vk130_assertion description "[In this review, we discuss three categories of genetic disease that highlight the importance of X-linked genes in the manifestation of an autistic phenotype: aneuploides (Turner syndrome and Klinefelter syndrome), trinucleotide expansions (Fragile X syndrome) and nucleotide mutations (Rett Syndrome, Neuroligins 3 & 4, and SLC6A8).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699592.RAaXeazEtGqMZbnvyPntT2rRiCYUDhiAKIegSkksyW9vk130_provenance.
- NP699592.RAaXeazEtGqMZbnvyPntT2rRiCYUDhiAKIegSkksyW9vk130_assertion evidence source_evidence_literature NP699592.RAaXeazEtGqMZbnvyPntT2rRiCYUDhiAKIegSkksyW9vk130_provenance.
- NP699592.RAaXeazEtGqMZbnvyPntT2rRiCYUDhiAKIegSkksyW9vk130_assertion SIO_000772 18985105 NP699592.RAaXeazEtGqMZbnvyPntT2rRiCYUDhiAKIegSkksyW9vk130_provenance.
- NP699592.RAaXeazEtGqMZbnvyPntT2rRiCYUDhiAKIegSkksyW9vk130_assertion wasDerivedFrom befree-20150227 NP699592.RAaXeazEtGqMZbnvyPntT2rRiCYUDhiAKIegSkksyW9vk130_provenance.
- NP699592.RAaXeazEtGqMZbnvyPntT2rRiCYUDhiAKIegSkksyW9vk130_assertion wasGeneratedBy ECO_0000203 NP699592.RAaXeazEtGqMZbnvyPntT2rRiCYUDhiAKIegSkksyW9vk130_provenance.