Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP502881.RAgQVmRmhG3PfCg3wpz2dZhy5GYj6-a540z8XYpi_nFPQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP502881.RAgQVmRmhG3PfCg3wpz2dZhy5GYj6-a540z8XYpi_nFPQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP502881.RAgQVmRmhG3PfCg3wpz2dZhy5GYj6-a540z8XYpi_nFPQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP502881.RAgQVmRmhG3PfCg3wpz2dZhy5GYj6-a540z8XYpi_nFPQ130_provenance.
- NP502881.RAgQVmRmhG3PfCg3wpz2dZhy5GYj6-a540z8XYpi_nFPQ130_assertion description "[The phenotype of the HID (hystrix-like ichthyosis, deafness)/KID (keratitis, ichthyosis, deafness) syndrome is primarily characterized by skin changes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502881.RAgQVmRmhG3PfCg3wpz2dZhy5GYj6-a540z8XYpi_nFPQ130_provenance.
- NP502881.RAgQVmRmhG3PfCg3wpz2dZhy5GYj6-a540z8XYpi_nFPQ130_assertion evidence source_evidence_literature NP502881.RAgQVmRmhG3PfCg3wpz2dZhy5GYj6-a540z8XYpi_nFPQ130_provenance.
- NP502881.RAgQVmRmhG3PfCg3wpz2dZhy5GYj6-a540z8XYpi_nFPQ130_assertion SIO_000772 16679758 NP502881.RAgQVmRmhG3PfCg3wpz2dZhy5GYj6-a540z8XYpi_nFPQ130_provenance.
- NP502881.RAgQVmRmhG3PfCg3wpz2dZhy5GYj6-a540z8XYpi_nFPQ130_assertion wasDerivedFrom befree-20140225 NP502881.RAgQVmRmhG3PfCg3wpz2dZhy5GYj6-a540z8XYpi_nFPQ130_provenance.
- NP502881.RAgQVmRmhG3PfCg3wpz2dZhy5GYj6-a540z8XYpi_nFPQ130_assertion wasGeneratedBy ECO_0000203 NP502881.RAgQVmRmhG3PfCg3wpz2dZhy5GYj6-a540z8XYpi_nFPQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP502881.RAgQVmRmhG3PfCg3wpz2dZhy5GYj6-a540z8XYpi_nFPQ130_provenance.