Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP437315.RADaAJ9he9-PdZqzFxdeP5jVh38xOAALBTltXrs3zsRJA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP437315.RADaAJ9he9-PdZqzFxdeP5jVh38xOAALBTltXrs3zsRJA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP437315.RADaAJ9he9-PdZqzFxdeP5jVh38xOAALBTltXrs3zsRJA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP437315.RADaAJ9he9-PdZqzFxdeP5jVh38xOAALBTltXrs3zsRJA130_provenance.
- NP437315.RADaAJ9he9-PdZqzFxdeP5jVh38xOAALBTltXrs3zsRJA130_assertion description "[Mutations in the transcription factor gene SOX18 cause vascular, lymphatic and hair follicle defects in humans with dominant and recessive forms of hypotrichosis-lymphedema-telangiectasia (HLT) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP437315.RADaAJ9he9-PdZqzFxdeP5jVh38xOAALBTltXrs3zsRJA130_provenance.
- NP437315.RADaAJ9he9-PdZqzFxdeP5jVh38xOAALBTltXrs3zsRJA130_assertion evidence source_evidence_literature NP437315.RADaAJ9he9-PdZqzFxdeP5jVh38xOAALBTltXrs3zsRJA130_provenance.
- NP437315.RADaAJ9he9-PdZqzFxdeP5jVh38xOAALBTltXrs3zsRJA130_assertion SIO_000772 19429912 NP437315.RADaAJ9he9-PdZqzFxdeP5jVh38xOAALBTltXrs3zsRJA130_provenance.
- NP437315.RADaAJ9he9-PdZqzFxdeP5jVh38xOAALBTltXrs3zsRJA130_assertion wasDerivedFrom befree-20140225 NP437315.RADaAJ9he9-PdZqzFxdeP5jVh38xOAALBTltXrs3zsRJA130_provenance.
- NP437315.RADaAJ9he9-PdZqzFxdeP5jVh38xOAALBTltXrs3zsRJA130_assertion wasGeneratedBy ECO_0000203 NP437315.RADaAJ9he9-PdZqzFxdeP5jVh38xOAALBTltXrs3zsRJA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP437315.RADaAJ9he9-PdZqzFxdeP5jVh38xOAALBTltXrs3zsRJA130_provenance.