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- source_evidence_literature type ECO_0000212 NP789748.RAfE72A18PZhkTwMS2vk6CIeEMC2sEKkSNLJrsjCXOYXg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP789748.RAfE72A18PZhkTwMS2vk6CIeEMC2sEKkSNLJrsjCXOYXg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP789748.RAfE72A18PZhkTwMS2vk6CIeEMC2sEKkSNLJrsjCXOYXg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP789748.RAfE72A18PZhkTwMS2vk6CIeEMC2sEKkSNLJrsjCXOYXg130_provenance.
- NP789748.RAfE72A18PZhkTwMS2vk6CIeEMC2sEKkSNLJrsjCXOYXg130_assertion wasGeneratedBy ECO_0000203 NP789748.RAfE72A18PZhkTwMS2vk6CIeEMC2sEKkSNLJrsjCXOYXg130_provenance.
- NP789748.RAfE72A18PZhkTwMS2vk6CIeEMC2sEKkSNLJrsjCXOYXg130_assertion wasDerivedFrom befree-20150227 NP789748.RAfE72A18PZhkTwMS2vk6CIeEMC2sEKkSNLJrsjCXOYXg130_provenance.
- NP789748.RAfE72A18PZhkTwMS2vk6CIeEMC2sEKkSNLJrsjCXOYXg130_assertion SIO_000772 21658225 NP789748.RAfE72A18PZhkTwMS2vk6CIeEMC2sEKkSNLJrsjCXOYXg130_provenance.
- NP789748.RAfE72A18PZhkTwMS2vk6CIeEMC2sEKkSNLJrsjCXOYXg130_assertion evidence source_evidence_literature NP789748.RAfE72A18PZhkTwMS2vk6CIeEMC2sEKkSNLJrsjCXOYXg130_provenance.
- NP789748.RAfE72A18PZhkTwMS2vk6CIeEMC2sEKkSNLJrsjCXOYXg130_assertion description "[The identification of a large spectrum of MLL2 mutations possibly offers the opportunity to improve the actual knowledge on the clinical basis of this multiple congenital anomalies/mental retardation syndrome, design functional studies to understand the molecular mechanisms underlying this disease, establish genotype-phenotype correlations and improve clinical management.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789748.RAfE72A18PZhkTwMS2vk6CIeEMC2sEKkSNLJrsjCXOYXg130_provenance.