Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP581961.RAA3Z52h0cm64_xZdQx3n7rJWQWSu6vka4dYmoXeF1KuQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP581961.RAA3Z52h0cm64_xZdQx3n7rJWQWSu6vka4dYmoXeF1KuQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP581961.RAA3Z52h0cm64_xZdQx3n7rJWQWSu6vka4dYmoXeF1KuQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP581961.RAA3Z52h0cm64_xZdQx3n7rJWQWSu6vka4dYmoXeF1KuQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP581961.RAA3Z52h0cm64_xZdQx3n7rJWQWSu6vka4dYmoXeF1KuQ130_provenance.
- NP581961.RAA3Z52h0cm64_xZdQx3n7rJWQWSu6vka4dYmoXeF1KuQ130_assertion wasGeneratedBy ECO_0000203 NP581961.RAA3Z52h0cm64_xZdQx3n7rJWQWSu6vka4dYmoXeF1KuQ130_provenance.
- NP581961.RAA3Z52h0cm64_xZdQx3n7rJWQWSu6vka4dYmoXeF1KuQ130_assertion wasDerivedFrom befree-2016 NP581961.RAA3Z52h0cm64_xZdQx3n7rJWQWSu6vka4dYmoXeF1KuQ130_provenance.
- NP581961.RAA3Z52h0cm64_xZdQx3n7rJWQWSu6vka4dYmoXeF1KuQ130_assertion SIO_000772 17139695 NP581961.RAA3Z52h0cm64_xZdQx3n7rJWQWSu6vka4dYmoXeF1KuQ130_provenance.
- NP581961.RAA3Z52h0cm64_xZdQx3n7rJWQWSu6vka4dYmoXeF1KuQ130_assertion evidence source_evidence_literature NP581961.RAA3Z52h0cm64_xZdQx3n7rJWQWSu6vka4dYmoXeF1KuQ130_provenance.
- NP581961.RAA3Z52h0cm64_xZdQx3n7rJWQWSu6vka4dYmoXeF1KuQ130_assertion description "[Eleven paternal diseases were discovered, which were Noonan-like syndrome (1), paternal cervical anomalies (1), Goldenhar syndrome (1), dominant autosomal arthrogryposis (1), osteogenesis imperfecta (3), tuberous sclerosis (1), dominant transposition of great vessels (1), Weyers acrofacial dysostosis (1), and autosomal dominant holoprosencephaly (1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581961.RAA3Z52h0cm64_xZdQx3n7rJWQWSu6vka4dYmoXeF1KuQ130_provenance.