Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP614349.RA-O7haWCME5m0mxu5jUoLYEDpv5nvGZ87aNFSBd1cW_0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP614349.RA-O7haWCME5m0mxu5jUoLYEDpv5nvGZ87aNFSBd1cW_0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP614349.RA-O7haWCME5m0mxu5jUoLYEDpv5nvGZ87aNFSBd1cW_0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP614349.RA-O7haWCME5m0mxu5jUoLYEDpv5nvGZ87aNFSBd1cW_0130_provenance.
- NP614349.RA-O7haWCME5m0mxu5jUoLYEDpv5nvGZ87aNFSBd1cW_0130_assertion description "[Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP614349.RA-O7haWCME5m0mxu5jUoLYEDpv5nvGZ87aNFSBd1cW_0130_provenance.
- NP614349.RA-O7haWCME5m0mxu5jUoLYEDpv5nvGZ87aNFSBd1cW_0130_assertion evidence source_evidence_literature NP614349.RA-O7haWCME5m0mxu5jUoLYEDpv5nvGZ87aNFSBd1cW_0130_provenance.
- NP614349.RA-O7haWCME5m0mxu5jUoLYEDpv5nvGZ87aNFSBd1cW_0130_assertion SIO_000772 20736978 NP614349.RA-O7haWCME5m0mxu5jUoLYEDpv5nvGZ87aNFSBd1cW_0130_provenance.
- NP614349.RA-O7haWCME5m0mxu5jUoLYEDpv5nvGZ87aNFSBd1cW_0130_assertion wasDerivedFrom befree-20140225 NP614349.RA-O7haWCME5m0mxu5jUoLYEDpv5nvGZ87aNFSBd1cW_0130_provenance.
- NP614349.RA-O7haWCME5m0mxu5jUoLYEDpv5nvGZ87aNFSBd1cW_0130_assertion wasGeneratedBy ECO_0000203 NP614349.RA-O7haWCME5m0mxu5jUoLYEDpv5nvGZ87aNFSBd1cW_0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP614349.RA-O7haWCME5m0mxu5jUoLYEDpv5nvGZ87aNFSBd1cW_0130_provenance.