Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_provenance.
- befree-2016 importedOn "2016-02-19" NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_provenance.
- NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_assertion wasGeneratedBy ECO_0000203 NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_provenance.
- NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_assertion wasDerivedFrom befree-2016 NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_provenance.
- NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_assertion SIO_000772 16550584 NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_provenance.
- NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_assertion evidence source_evidence_literature NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_provenance.
- NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_assertion description "[Similarly, allelsim in the gene encoding wolframin (WFS1) causes either a nonsyndromic dominant low-frequency hearing loss (DFNA6/14/38) or Wolfram syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_provenance.