Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_provenance.
- NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_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." NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_provenance.
- NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_assertion evidence source_evidence_literature NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_provenance.
- NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_assertion SIO_000772 16845484 NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_provenance.
- NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_assertion wasDerivedFrom befree-2016 NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_provenance.
- NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_assertion wasGeneratedBy ECO_0000203 NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_provenance.
- befree-2016 importedOn "2016-02-19" NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_provenance.