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- source_evidence_literature type ECO_0000212 NP409251.RAc801iuLBw_0X-CAi5iumt8xz4_KFRDw5W5EraKBEQfI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP409251.RAc801iuLBw_0X-CAi5iumt8xz4_KFRDw5W5EraKBEQfI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP409251.RAc801iuLBw_0X-CAi5iumt8xz4_KFRDw5W5EraKBEQfI130_provenance.
- NP409251.RAc801iuLBw_0X-CAi5iumt8xz4_KFRDw5W5EraKBEQfI130_assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409251.RAc801iuLBw_0X-CAi5iumt8xz4_KFRDw5W5EraKBEQfI130_provenance.
- NP409251.RAc801iuLBw_0X-CAi5iumt8xz4_KFRDw5W5EraKBEQfI130_assertion evidence source_evidence_literature NP409251.RAc801iuLBw_0X-CAi5iumt8xz4_KFRDw5W5EraKBEQfI130_provenance.
- NP409251.RAc801iuLBw_0X-CAi5iumt8xz4_KFRDw5W5EraKBEQfI130_assertion SIO_000772 11309367 NP409251.RAc801iuLBw_0X-CAi5iumt8xz4_KFRDw5W5EraKBEQfI130_provenance.
- NP409251.RAc801iuLBw_0X-CAi5iumt8xz4_KFRDw5W5EraKBEQfI130_assertion wasDerivedFrom befree-20150227 NP409251.RAc801iuLBw_0X-CAi5iumt8xz4_KFRDw5W5EraKBEQfI130_provenance.
- NP409251.RAc801iuLBw_0X-CAi5iumt8xz4_KFRDw5W5EraKBEQfI130_assertion wasGeneratedBy ECO_0000203 NP409251.RAc801iuLBw_0X-CAi5iumt8xz4_KFRDw5W5EraKBEQfI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP409251.RAc801iuLBw_0X-CAi5iumt8xz4_KFRDw5W5EraKBEQfI130_provenance.