Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP199320.RA3AIp3e5_hoIlgEduT2MKhJm4sUCcMFfopOwulTlGeto130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP199320.RA3AIp3e5_hoIlgEduT2MKhJm4sUCcMFfopOwulTlGeto130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP199320.RA3AIp3e5_hoIlgEduT2MKhJm4sUCcMFfopOwulTlGeto130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP199320.RA3AIp3e5_hoIlgEduT2MKhJm4sUCcMFfopOwulTlGeto130_provenance.
- NP199320.RA3AIp3e5_hoIlgEduT2MKhJm4sUCcMFfopOwulTlGeto130_assertion description "[connexin 26 mutations are linked to sensorineural hearing loss in children]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199320.RA3AIp3e5_hoIlgEduT2MKhJm4sUCcMFfopOwulTlGeto130_provenance.
- NP199320.RA3AIp3e5_hoIlgEduT2MKhJm4sUCcMFfopOwulTlGeto130_assertion evidence source_evidence_literature NP199320.RA3AIp3e5_hoIlgEduT2MKhJm4sUCcMFfopOwulTlGeto130_provenance.
- NP199320.RA3AIp3e5_hoIlgEduT2MKhJm4sUCcMFfopOwulTlGeto130_assertion SIO_000772 15064611 NP199320.RA3AIp3e5_hoIlgEduT2MKhJm4sUCcMFfopOwulTlGeto130_provenance.
- NP199320.RA3AIp3e5_hoIlgEduT2MKhJm4sUCcMFfopOwulTlGeto130_assertion wasDerivedFrom lhgdn-20090331 NP199320.RA3AIp3e5_hoIlgEduT2MKhJm4sUCcMFfopOwulTlGeto130_provenance.
- NP199320.RA3AIp3e5_hoIlgEduT2MKhJm4sUCcMFfopOwulTlGeto130_assertion wasGeneratedBy ECO_0000203 NP199320.RA3AIp3e5_hoIlgEduT2MKhJm4sUCcMFfopOwulTlGeto130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP199320.RA3AIp3e5_hoIlgEduT2MKhJm4sUCcMFfopOwulTlGeto130_provenance.