Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP164467.RAVnWCh2A10yI-rTrrBgBSpeGzoroa4gVHpWrYy_J3b78130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP164467.RAVnWCh2A10yI-rTrrBgBSpeGzoroa4gVHpWrYy_J3b78130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP164467.RAVnWCh2A10yI-rTrrBgBSpeGzoroa4gVHpWrYy_J3b78130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP164467.RAVnWCh2A10yI-rTrrBgBSpeGzoroa4gVHpWrYy_J3b78130_provenance.
- NP164467.RAVnWCh2A10yI-rTrrBgBSpeGzoroa4gVHpWrYy_J3b78130_assertion description "[Phenotype in GJB2-associated hearing loss is correlated with genotype, with truncating mutations giving rise to more severe hearing loss. Progression of hearing loss is not uncommon, especially in association with the p.V37I allele. These results suggest ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164467.RAVnWCh2A10yI-rTrrBgBSpeGzoroa4gVHpWrYy_J3b78130_provenance.
- NP164467.RAVnWCh2A10yI-rTrrBgBSpeGzoroa4gVHpWrYy_J3b78130_assertion evidence source_evidence_literature NP164467.RAVnWCh2A10yI-rTrrBgBSpeGzoroa4gVHpWrYy_J3b78130_provenance.
- NP164467.RAVnWCh2A10yI-rTrrBgBSpeGzoroa4gVHpWrYy_J3b78130_assertion SIO_000772 20154630 NP164467.RAVnWCh2A10yI-rTrrBgBSpeGzoroa4gVHpWrYy_J3b78130_provenance.
- NP164467.RAVnWCh2A10yI-rTrrBgBSpeGzoroa4gVHpWrYy_J3b78130_assertion wasDerivedFrom gad-20150221 NP164467.RAVnWCh2A10yI-rTrrBgBSpeGzoroa4gVHpWrYy_J3b78130_provenance.
- NP164467.RAVnWCh2A10yI-rTrrBgBSpeGzoroa4gVHpWrYy_J3b78130_assertion wasGeneratedBy ECO_0000203 NP164467.RAVnWCh2A10yI-rTrrBgBSpeGzoroa4gVHpWrYy_J3b78130_provenance.
- gad-20150221 importedOn "2015-02-21" NP164467.RAVnWCh2A10yI-rTrrBgBSpeGzoroa4gVHpWrYy_J3b78130_provenance.