Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP385877.RAQm-HT2NPXxIMMot19L9v9cQfGwcj25p5QolY47-I0_Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP385877.RAQm-HT2NPXxIMMot19L9v9cQfGwcj25p5QolY47-I0_Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP385877.RAQm-HT2NPXxIMMot19L9v9cQfGwcj25p5QolY47-I0_Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP385877.RAQm-HT2NPXxIMMot19L9v9cQfGwcj25p5QolY47-I0_Y130_provenance.
- NP385877.RAQm-HT2NPXxIMMot19L9v9cQfGwcj25p5QolY47-I0_Y130_assertion description "[Mutations in the human ARX gene have been shown to cause nonsyndromic X-linked mental retardation (MRX) as well as syndromic forms such as X-linked lissencephaly with abnormal genitalia (XLAG), Partington syndrome and X-linked infantile spasm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP385877.RAQm-HT2NPXxIMMot19L9v9cQfGwcj25p5QolY47-I0_Y130_provenance.
- NP385877.RAQm-HT2NPXxIMMot19L9v9cQfGwcj25p5QolY47-I0_Y130_assertion evidence source_evidence_literature NP385877.RAQm-HT2NPXxIMMot19L9v9cQfGwcj25p5QolY47-I0_Y130_provenance.
- NP385877.RAQm-HT2NPXxIMMot19L9v9cQfGwcj25p5QolY47-I0_Y130_assertion SIO_000772 16235064 NP385877.RAQm-HT2NPXxIMMot19L9v9cQfGwcj25p5QolY47-I0_Y130_provenance.
- NP385877.RAQm-HT2NPXxIMMot19L9v9cQfGwcj25p5QolY47-I0_Y130_assertion wasDerivedFrom befree-20140225 NP385877.RAQm-HT2NPXxIMMot19L9v9cQfGwcj25p5QolY47-I0_Y130_provenance.
- NP385877.RAQm-HT2NPXxIMMot19L9v9cQfGwcj25p5QolY47-I0_Y130_assertion wasGeneratedBy ECO_0000203 NP385877.RAQm-HT2NPXxIMMot19L9v9cQfGwcj25p5QolY47-I0_Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP385877.RAQm-HT2NPXxIMMot19L9v9cQfGwcj25p5QolY47-I0_Y130_provenance.