Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP195193.RAnUWI0qAv_lRrzBCo0Qh67C6s0FuEyKaBJsneBCyit_s130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP195193.RAnUWI0qAv_lRrzBCo0Qh67C6s0FuEyKaBJsneBCyit_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP195193.RAnUWI0qAv_lRrzBCo0Qh67C6s0FuEyKaBJsneBCyit_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP195193.RAnUWI0qAv_lRrzBCo0Qh67C6s0FuEyKaBJsneBCyit_s130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP195193.RAnUWI0qAv_lRrzBCo0Qh67C6s0FuEyKaBJsneBCyit_s130_provenance.
- NP195193.RAnUWI0qAv_lRrzBCo0Qh67C6s0FuEyKaBJsneBCyit_s130_assertion wasGeneratedBy ECO_0000203 NP195193.RAnUWI0qAv_lRrzBCo0Qh67C6s0FuEyKaBJsneBCyit_s130_provenance.
- NP195193.RAnUWI0qAv_lRrzBCo0Qh67C6s0FuEyKaBJsneBCyit_s130_assertion wasDerivedFrom lhgdn-20090331 NP195193.RAnUWI0qAv_lRrzBCo0Qh67C6s0FuEyKaBJsneBCyit_s130_provenance.
- NP195193.RAnUWI0qAv_lRrzBCo0Qh67C6s0FuEyKaBJsneBCyit_s130_assertion SIO_000772 12107438 NP195193.RAnUWI0qAv_lRrzBCo0Qh67C6s0FuEyKaBJsneBCyit_s130_provenance.
- NP195193.RAnUWI0qAv_lRrzBCo0Qh67C6s0FuEyKaBJsneBCyit_s130_assertion evidence source_evidence_literature NP195193.RAnUWI0qAv_lRrzBCo0Qh67C6s0FuEyKaBJsneBCyit_s130_provenance.
- NP195193.RAnUWI0qAv_lRrzBCo0Qh67C6s0FuEyKaBJsneBCyit_s130_assertion description "[Mutations of USHIC can cause both Usher syndrome type IC and nonsyndromic recessive deafness DFNB18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP195193.RAnUWI0qAv_lRrzBCo0Qh67C6s0FuEyKaBJsneBCyit_s130_provenance.