Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP894670.RArwiS7ltkbePLdwk0_wjwX9KtDw758elMTfaDHkQ4wYY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP894670.RArwiS7ltkbePLdwk0_wjwX9KtDw758elMTfaDHkQ4wYY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP894670.RArwiS7ltkbePLdwk0_wjwX9KtDw758elMTfaDHkQ4wYY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP894670.RArwiS7ltkbePLdwk0_wjwX9KtDw758elMTfaDHkQ4wYY130_provenance.
- NP894670.RArwiS7ltkbePLdwk0_wjwX9KtDw758elMTfaDHkQ4wYY130_assertion description "[Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP894670.RArwiS7ltkbePLdwk0_wjwX9KtDw758elMTfaDHkQ4wYY130_provenance.
- NP894670.RArwiS7ltkbePLdwk0_wjwX9KtDw758elMTfaDHkQ4wYY130_assertion evidence source_evidence_literature NP894670.RArwiS7ltkbePLdwk0_wjwX9KtDw758elMTfaDHkQ4wYY130_provenance.
- NP894670.RArwiS7ltkbePLdwk0_wjwX9KtDw758elMTfaDHkQ4wYY130_assertion SIO_000772 20602914 NP894670.RArwiS7ltkbePLdwk0_wjwX9KtDw758elMTfaDHkQ4wYY130_provenance.
- NP894670.RArwiS7ltkbePLdwk0_wjwX9KtDw758elMTfaDHkQ4wYY130_assertion wasDerivedFrom befree-20150227 NP894670.RArwiS7ltkbePLdwk0_wjwX9KtDw758elMTfaDHkQ4wYY130_provenance.
- NP894670.RArwiS7ltkbePLdwk0_wjwX9KtDw758elMTfaDHkQ4wYY130_assertion wasGeneratedBy ECO_0000203 NP894670.RArwiS7ltkbePLdwk0_wjwX9KtDw758elMTfaDHkQ4wYY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP894670.RArwiS7ltkbePLdwk0_wjwX9KtDw758elMTfaDHkQ4wYY130_provenance.