Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP704429.RANFp3T5k5asWg02Dfi2gmwJTmycljglsSaW1XfCwOPFw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP704429.RANFp3T5k5asWg02Dfi2gmwJTmycljglsSaW1XfCwOPFw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP704429.RANFp3T5k5asWg02Dfi2gmwJTmycljglsSaW1XfCwOPFw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP704429.RANFp3T5k5asWg02Dfi2gmwJTmycljglsSaW1XfCwOPFw130_provenance.
- NP704429.RANFp3T5k5asWg02Dfi2gmwJTmycljglsSaW1XfCwOPFw130_assertion wasGeneratedBy ECO_0000203 NP704429.RANFp3T5k5asWg02Dfi2gmwJTmycljglsSaW1XfCwOPFw130_provenance.
- NP704429.RANFp3T5k5asWg02Dfi2gmwJTmycljglsSaW1XfCwOPFw130_assertion wasDerivedFrom befree-20140225 NP704429.RANFp3T5k5asWg02Dfi2gmwJTmycljglsSaW1XfCwOPFw130_provenance.
- NP704429.RANFp3T5k5asWg02Dfi2gmwJTmycljglsSaW1XfCwOPFw130_assertion SIO_000772 12107438 NP704429.RANFp3T5k5asWg02Dfi2gmwJTmycljglsSaW1XfCwOPFw130_provenance.
- NP704429.RANFp3T5k5asWg02Dfi2gmwJTmycljglsSaW1XfCwOPFw130_assertion evidence source_evidence_literature NP704429.RANFp3T5k5asWg02Dfi2gmwJTmycljglsSaW1XfCwOPFw130_provenance.
- NP704429.RANFp3T5k5asWg02Dfi2gmwJTmycljglsSaW1XfCwOPFw130_assertion description "[We conclude that 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." NP704429.RANFp3T5k5asWg02Dfi2gmwJTmycljglsSaW1XfCwOPFw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP704429.RANFp3T5k5asWg02Dfi2gmwJTmycljglsSaW1XfCwOPFw130_provenance.