Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP295371.RAESWKpkuG8Xmv-l3_y8UEQf4BmWrWZCzh2ZsspJqlt5c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP295371.RAESWKpkuG8Xmv-l3_y8UEQf4BmWrWZCzh2ZsspJqlt5c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP295371.RAESWKpkuG8Xmv-l3_y8UEQf4BmWrWZCzh2ZsspJqlt5c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP295371.RAESWKpkuG8Xmv-l3_y8UEQf4BmWrWZCzh2ZsspJqlt5c130_provenance.
- NP295371.RAESWKpkuG8Xmv-l3_y8UEQf4BmWrWZCzh2ZsspJqlt5c130_assertion description "[Mutations in the ATR-X gene (ATRX) that encodes a putative global transcription factor have been identified in patients with ATR-X as well as those with other forms of X-linked mental retardation syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP295371.RAESWKpkuG8Xmv-l3_y8UEQf4BmWrWZCzh2ZsspJqlt5c130_provenance.
- NP295371.RAESWKpkuG8Xmv-l3_y8UEQf4BmWrWZCzh2ZsspJqlt5c130_assertion evidence source_evidence_literature NP295371.RAESWKpkuG8Xmv-l3_y8UEQf4BmWrWZCzh2ZsspJqlt5c130_provenance.
- NP295371.RAESWKpkuG8Xmv-l3_y8UEQf4BmWrWZCzh2ZsspJqlt5c130_assertion SIO_000772 10995512 NP295371.RAESWKpkuG8Xmv-l3_y8UEQf4BmWrWZCzh2ZsspJqlt5c130_provenance.
- NP295371.RAESWKpkuG8Xmv-l3_y8UEQf4BmWrWZCzh2ZsspJqlt5c130_assertion wasDerivedFrom befree-2016 NP295371.RAESWKpkuG8Xmv-l3_y8UEQf4BmWrWZCzh2ZsspJqlt5c130_provenance.
- NP295371.RAESWKpkuG8Xmv-l3_y8UEQf4BmWrWZCzh2ZsspJqlt5c130_assertion wasGeneratedBy ECO_0000203 NP295371.RAESWKpkuG8Xmv-l3_y8UEQf4BmWrWZCzh2ZsspJqlt5c130_provenance.
- befree-2016 importedOn "2016-02-19" NP295371.RAESWKpkuG8Xmv-l3_y8UEQf4BmWrWZCzh2ZsspJqlt5c130_provenance.