Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP606198.RAAO_p1zFV7huSASH2MznM76vjzY6xAHiHqXuRS9El1YA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP606198.RAAO_p1zFV7huSASH2MznM76vjzY6xAHiHqXuRS9El1YA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP606198.RAAO_p1zFV7huSASH2MznM76vjzY6xAHiHqXuRS9El1YA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP606198.RAAO_p1zFV7huSASH2MznM76vjzY6xAHiHqXuRS9El1YA130_provenance.
- NP606198.RAAO_p1zFV7huSASH2MznM76vjzY6xAHiHqXuRS9El1YA130_assertion description "[Most children have severe developmental delay and infantile spasms, but milder phenotypes are on record, including posterior subcortical band heterotopia owing to mosaic mutations of LIS1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606198.RAAO_p1zFV7huSASH2MznM76vjzY6xAHiHqXuRS9El1YA130_provenance.
- NP606198.RAAO_p1zFV7huSASH2MznM76vjzY6xAHiHqXuRS9El1YA130_assertion evidence source_evidence_literature NP606198.RAAO_p1zFV7huSASH2MznM76vjzY6xAHiHqXuRS9El1YA130_provenance.
- NP606198.RAAO_p1zFV7huSASH2MznM76vjzY6xAHiHqXuRS9El1YA130_assertion SIO_000772 15921228 NP606198.RAAO_p1zFV7huSASH2MznM76vjzY6xAHiHqXuRS9El1YA130_provenance.
- NP606198.RAAO_p1zFV7huSASH2MznM76vjzY6xAHiHqXuRS9El1YA130_assertion wasDerivedFrom befree-20150227 NP606198.RAAO_p1zFV7huSASH2MznM76vjzY6xAHiHqXuRS9El1YA130_provenance.
- NP606198.RAAO_p1zFV7huSASH2MznM76vjzY6xAHiHqXuRS9El1YA130_assertion wasGeneratedBy ECO_0000203 NP606198.RAAO_p1zFV7huSASH2MznM76vjzY6xAHiHqXuRS9El1YA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP606198.RAAO_p1zFV7huSASH2MznM76vjzY6xAHiHqXuRS9El1YA130_provenance.