Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP815721.RARNASmc_5iI1HDuBaU3_F7sa_bQrBv72GcX9WK-ewV_4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP815721.RARNASmc_5iI1HDuBaU3_F7sa_bQrBv72GcX9WK-ewV_4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP815721.RARNASmc_5iI1HDuBaU3_F7sa_bQrBv72GcX9WK-ewV_4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP815721.RARNASmc_5iI1HDuBaU3_F7sa_bQrBv72GcX9WK-ewV_4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP815721.RARNASmc_5iI1HDuBaU3_F7sa_bQrBv72GcX9WK-ewV_4130_provenance.
- NP815721.RARNASmc_5iI1HDuBaU3_F7sa_bQrBv72GcX9WK-ewV_4130_assertion wasGeneratedBy ECO_0000203 NP815721.RARNASmc_5iI1HDuBaU3_F7sa_bQrBv72GcX9WK-ewV_4130_provenance.
- NP815721.RARNASmc_5iI1HDuBaU3_F7sa_bQrBv72GcX9WK-ewV_4130_assertion wasDerivedFrom befree-20150227 NP815721.RARNASmc_5iI1HDuBaU3_F7sa_bQrBv72GcX9WK-ewV_4130_provenance.
- NP815721.RARNASmc_5iI1HDuBaU3_F7sa_bQrBv72GcX9WK-ewV_4130_assertion SIO_000772 10925378 NP815721.RARNASmc_5iI1HDuBaU3_F7sa_bQrBv72GcX9WK-ewV_4130_provenance.
- NP815721.RARNASmc_5iI1HDuBaU3_F7sa_bQrBv72GcX9WK-ewV_4130_assertion evidence source_evidence_literature NP815721.RARNASmc_5iI1HDuBaU3_F7sa_bQrBv72GcX9WK-ewV_4130_provenance.
- NP815721.RARNASmc_5iI1HDuBaU3_F7sa_bQrBv72GcX9WK-ewV_4130_assertion description "[The DFNA2 locus for autosomal dominant nonsyndromic hearing impairment on chromosome 1p34 contains at least 2 genes responsible for hearing loss, GJB3 and KCNQ4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP815721.RARNASmc_5iI1HDuBaU3_F7sa_bQrBv72GcX9WK-ewV_4130_provenance.