Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP75688.RA6EI8KXnlfwOxci_2euEAeRd5SFlo4LZtmO9v1vV6mTQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP75688.RA6EI8KXnlfwOxci_2euEAeRd5SFlo4LZtmO9v1vV6mTQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP75688.RA6EI8KXnlfwOxci_2euEAeRd5SFlo4LZtmO9v1vV6mTQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP75688.RA6EI8KXnlfwOxci_2euEAeRd5SFlo4LZtmO9v1vV6mTQ130_provenance.
- NP75688.RA6EI8KXnlfwOxci_2euEAeRd5SFlo4LZtmO9v1vV6mTQ130_assertion description "[Considering the very large size of the USH2A gene and the high number of mutations detected in USH2 patients worldwide, our findings have significant implications for genetic counseling and carrier screening in various Jewish populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP75688.RA6EI8KXnlfwOxci_2euEAeRd5SFlo4LZtmO9v1vV6mTQ130_provenance.
- NP75688.RA6EI8KXnlfwOxci_2euEAeRd5SFlo4LZtmO9v1vV6mTQ130_assertion evidence source_evidence_literature NP75688.RA6EI8KXnlfwOxci_2euEAeRd5SFlo4LZtmO9v1vV6mTQ130_provenance.
- NP75688.RA6EI8KXnlfwOxci_2euEAeRd5SFlo4LZtmO9v1vV6mTQ130_assertion SIO_000772 18452394 NP75688.RA6EI8KXnlfwOxci_2euEAeRd5SFlo4LZtmO9v1vV6mTQ130_provenance.
- NP75688.RA6EI8KXnlfwOxci_2euEAeRd5SFlo4LZtmO9v1vV6mTQ130_assertion wasDerivedFrom gad-20150221 NP75688.RA6EI8KXnlfwOxci_2euEAeRd5SFlo4LZtmO9v1vV6mTQ130_provenance.
- NP75688.RA6EI8KXnlfwOxci_2euEAeRd5SFlo4LZtmO9v1vV6mTQ130_assertion wasGeneratedBy ECO_0000203 NP75688.RA6EI8KXnlfwOxci_2euEAeRd5SFlo4LZtmO9v1vV6mTQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP75688.RA6EI8KXnlfwOxci_2euEAeRd5SFlo4LZtmO9v1vV6mTQ130_provenance.