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- source_evidence_literature type ECO_0000212 NP699592.RAaXeazEtGqMZbnvyPntT2rRiCYUDhiAKIegSkksyW9vk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP699592.RAaXeazEtGqMZbnvyPntT2rRiCYUDhiAKIegSkksyW9vk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP699592.RAaXeazEtGqMZbnvyPntT2rRiCYUDhiAKIegSkksyW9vk130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP699592.RAaXeazEtGqMZbnvyPntT2rRiCYUDhiAKIegSkksyW9vk130_provenance.