Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP681043.RAlqgB2dRxRYNcvt4F9NHmZF1tU378iSSBSKiRB6mVonY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP681043.RAlqgB2dRxRYNcvt4F9NHmZF1tU378iSSBSKiRB6mVonY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681043.RAlqgB2dRxRYNcvt4F9NHmZF1tU378iSSBSKiRB6mVonY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681043.RAlqgB2dRxRYNcvt4F9NHmZF1tU378iSSBSKiRB6mVonY130_provenance.
- NP681043.RAlqgB2dRxRYNcvt4F9NHmZF1tU378iSSBSKiRB6mVonY130_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." NP681043.RAlqgB2dRxRYNcvt4F9NHmZF1tU378iSSBSKiRB6mVonY130_provenance.
- NP681043.RAlqgB2dRxRYNcvt4F9NHmZF1tU378iSSBSKiRB6mVonY130_assertion evidence source_evidence_literature NP681043.RAlqgB2dRxRYNcvt4F9NHmZF1tU378iSSBSKiRB6mVonY130_provenance.
- NP681043.RAlqgB2dRxRYNcvt4F9NHmZF1tU378iSSBSKiRB6mVonY130_assertion SIO_000772 16845484 NP681043.RAlqgB2dRxRYNcvt4F9NHmZF1tU378iSSBSKiRB6mVonY130_provenance.
- NP681043.RAlqgB2dRxRYNcvt4F9NHmZF1tU378iSSBSKiRB6mVonY130_assertion wasDerivedFrom befree-20140225 NP681043.RAlqgB2dRxRYNcvt4F9NHmZF1tU378iSSBSKiRB6mVonY130_provenance.
- NP681043.RAlqgB2dRxRYNcvt4F9NHmZF1tU378iSSBSKiRB6mVonY130_assertion wasGeneratedBy ECO_0000203 NP681043.RAlqgB2dRxRYNcvt4F9NHmZF1tU378iSSBSKiRB6mVonY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP681043.RAlqgB2dRxRYNcvt4F9NHmZF1tU378iSSBSKiRB6mVonY130_provenance.