Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978110.RA3FReeVE-2K94GlOq2AdfcDFOvfgqQ7gcCMIxmnwRcCg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978110.RA3FReeVE-2K94GlOq2AdfcDFOvfgqQ7gcCMIxmnwRcCg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978110.RA3FReeVE-2K94GlOq2AdfcDFOvfgqQ7gcCMIxmnwRcCg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978110.RA3FReeVE-2K94GlOq2AdfcDFOvfgqQ7gcCMIxmnwRcCg130_provenance.
- NP978110.RA3FReeVE-2K94GlOq2AdfcDFOvfgqQ7gcCMIxmnwRcCg130_assertion description "[ARX gene mutations have been known as important causes of developmental and neurological disorders and are responsible for a large spectrum of abnormal phenotypes, includeing syndromic as well as nonsyndromic forms of mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978110.RA3FReeVE-2K94GlOq2AdfcDFOvfgqQ7gcCMIxmnwRcCg130_provenance.
- NP978110.RA3FReeVE-2K94GlOq2AdfcDFOvfgqQ7gcCMIxmnwRcCg130_assertion evidence source_evidence_literature NP978110.RA3FReeVE-2K94GlOq2AdfcDFOvfgqQ7gcCMIxmnwRcCg130_provenance.
- NP978110.RA3FReeVE-2K94GlOq2AdfcDFOvfgqQ7gcCMIxmnwRcCg130_assertion SIO_000772 16845484 NP978110.RA3FReeVE-2K94GlOq2AdfcDFOvfgqQ7gcCMIxmnwRcCg130_provenance.
- NP978110.RA3FReeVE-2K94GlOq2AdfcDFOvfgqQ7gcCMIxmnwRcCg130_assertion wasDerivedFrom befree-20150227 NP978110.RA3FReeVE-2K94GlOq2AdfcDFOvfgqQ7gcCMIxmnwRcCg130_provenance.
- NP978110.RA3FReeVE-2K94GlOq2AdfcDFOvfgqQ7gcCMIxmnwRcCg130_assertion wasGeneratedBy ECO_0000203 NP978110.RA3FReeVE-2K94GlOq2AdfcDFOvfgqQ7gcCMIxmnwRcCg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978110.RA3FReeVE-2K94GlOq2AdfcDFOvfgqQ7gcCMIxmnwRcCg130_provenance.