Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP552231.RAsW23qcGVm-H9L2KHW7M70o5Kyk-S2wPP-mwRIFJOLS8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP552231.RAsW23qcGVm-H9L2KHW7M70o5Kyk-S2wPP-mwRIFJOLS8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP552231.RAsW23qcGVm-H9L2KHW7M70o5Kyk-S2wPP-mwRIFJOLS8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP552231.RAsW23qcGVm-H9L2KHW7M70o5Kyk-S2wPP-mwRIFJOLS8130_provenance.
- NP552231.RAsW23qcGVm-H9L2KHW7M70o5Kyk-S2wPP-mwRIFJOLS8130_assertion description "[MECP2 mutations or altered expression are also associated with a spectrum of neurodevelopmental disorders such as autism spectrum disorders with recent links to fetal alcohol spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552231.RAsW23qcGVm-H9L2KHW7M70o5Kyk-S2wPP-mwRIFJOLS8130_provenance.
- NP552231.RAsW23qcGVm-H9L2KHW7M70o5Kyk-S2wPP-mwRIFJOLS8130_assertion evidence source_evidence_literature NP552231.RAsW23qcGVm-H9L2KHW7M70o5Kyk-S2wPP-mwRIFJOLS8130_provenance.
- NP552231.RAsW23qcGVm-H9L2KHW7M70o5Kyk-S2wPP-mwRIFJOLS8130_assertion SIO_000772 24615633 NP552231.RAsW23qcGVm-H9L2KHW7M70o5Kyk-S2wPP-mwRIFJOLS8130_provenance.
- NP552231.RAsW23qcGVm-H9L2KHW7M70o5Kyk-S2wPP-mwRIFJOLS8130_assertion wasDerivedFrom befree-20150227 NP552231.RAsW23qcGVm-H9L2KHW7M70o5Kyk-S2wPP-mwRIFJOLS8130_provenance.
- NP552231.RAsW23qcGVm-H9L2KHW7M70o5Kyk-S2wPP-mwRIFJOLS8130_assertion wasGeneratedBy ECO_0000203 NP552231.RAsW23qcGVm-H9L2KHW7M70o5Kyk-S2wPP-mwRIFJOLS8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP552231.RAsW23qcGVm-H9L2KHW7M70o5Kyk-S2wPP-mwRIFJOLS8130_provenance.