Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP424766.RAedvzed7tKow1IBgwHyrvPT1m25UwWkjh6_pvNFNdAxo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP424766.RAedvzed7tKow1IBgwHyrvPT1m25UwWkjh6_pvNFNdAxo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP424766.RAedvzed7tKow1IBgwHyrvPT1m25UwWkjh6_pvNFNdAxo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP424766.RAedvzed7tKow1IBgwHyrvPT1m25UwWkjh6_pvNFNdAxo130_provenance.
- NP424766.RAedvzed7tKow1IBgwHyrvPT1m25UwWkjh6_pvNFNdAxo130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP424766.RAedvzed7tKow1IBgwHyrvPT1m25UwWkjh6_pvNFNdAxo130_provenance.
- NP424766.RAedvzed7tKow1IBgwHyrvPT1m25UwWkjh6_pvNFNdAxo130_assertion evidence source_evidence_literature NP424766.RAedvzed7tKow1IBgwHyrvPT1m25UwWkjh6_pvNFNdAxo130_provenance.
- NP424766.RAedvzed7tKow1IBgwHyrvPT1m25UwWkjh6_pvNFNdAxo130_assertion SIO_000772 8744027 NP424766.RAedvzed7tKow1IBgwHyrvPT1m25UwWkjh6_pvNFNdAxo130_provenance.
- NP424766.RAedvzed7tKow1IBgwHyrvPT1m25UwWkjh6_pvNFNdAxo130_assertion wasDerivedFrom befree-20140225 NP424766.RAedvzed7tKow1IBgwHyrvPT1m25UwWkjh6_pvNFNdAxo130_provenance.
- NP424766.RAedvzed7tKow1IBgwHyrvPT1m25UwWkjh6_pvNFNdAxo130_assertion wasGeneratedBy ECO_0000203 NP424766.RAedvzed7tKow1IBgwHyrvPT1m25UwWkjh6_pvNFNdAxo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP424766.RAedvzed7tKow1IBgwHyrvPT1m25UwWkjh6_pvNFNdAxo130_provenance.