Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP535038.RALdngTYRXOwt6n3oYXyp3ErK2WuwTuUC-3kn-l4zxp-s130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP535038.RALdngTYRXOwt6n3oYXyp3ErK2WuwTuUC-3kn-l4zxp-s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP535038.RALdngTYRXOwt6n3oYXyp3ErK2WuwTuUC-3kn-l4zxp-s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP535038.RALdngTYRXOwt6n3oYXyp3ErK2WuwTuUC-3kn-l4zxp-s130_provenance.
- NP535038.RALdngTYRXOwt6n3oYXyp3ErK2WuwTuUC-3kn-l4zxp-s130_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." NP535038.RALdngTYRXOwt6n3oYXyp3ErK2WuwTuUC-3kn-l4zxp-s130_provenance.
- NP535038.RALdngTYRXOwt6n3oYXyp3ErK2WuwTuUC-3kn-l4zxp-s130_assertion evidence source_evidence_literature NP535038.RALdngTYRXOwt6n3oYXyp3ErK2WuwTuUC-3kn-l4zxp-s130_provenance.
- NP535038.RALdngTYRXOwt6n3oYXyp3ErK2WuwTuUC-3kn-l4zxp-s130_assertion SIO_000772 16679758 NP535038.RALdngTYRXOwt6n3oYXyp3ErK2WuwTuUC-3kn-l4zxp-s130_provenance.
- NP535038.RALdngTYRXOwt6n3oYXyp3ErK2WuwTuUC-3kn-l4zxp-s130_assertion wasDerivedFrom befree-20140225 NP535038.RALdngTYRXOwt6n3oYXyp3ErK2WuwTuUC-3kn-l4zxp-s130_provenance.
- NP535038.RALdngTYRXOwt6n3oYXyp3ErK2WuwTuUC-3kn-l4zxp-s130_assertion wasGeneratedBy ECO_0000203 NP535038.RALdngTYRXOwt6n3oYXyp3ErK2WuwTuUC-3kn-l4zxp-s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP535038.RALdngTYRXOwt6n3oYXyp3ErK2WuwTuUC-3kn-l4zxp-s130_provenance.