Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP447490.RA1poHgfVKXwPScFoV0EfFW1p7U4HdEUsGwpu1vHn72dw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP447490.RA1poHgfVKXwPScFoV0EfFW1p7U4HdEUsGwpu1vHn72dw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP447490.RA1poHgfVKXwPScFoV0EfFW1p7U4HdEUsGwpu1vHn72dw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP447490.RA1poHgfVKXwPScFoV0EfFW1p7U4HdEUsGwpu1vHn72dw130_provenance.
- NP447490.RA1poHgfVKXwPScFoV0EfFW1p7U4HdEUsGwpu1vHn72dw130_assertion description "[MYH9-related disorders may be associated with deafness and cataract; hence, Alport syndrome becomes important in the differential diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP447490.RA1poHgfVKXwPScFoV0EfFW1p7U4HdEUsGwpu1vHn72dw130_provenance.
- NP447490.RA1poHgfVKXwPScFoV0EfFW1p7U4HdEUsGwpu1vHn72dw130_assertion evidence source_evidence_literature NP447490.RA1poHgfVKXwPScFoV0EfFW1p7U4HdEUsGwpu1vHn72dw130_provenance.
- NP447490.RA1poHgfVKXwPScFoV0EfFW1p7U4HdEUsGwpu1vHn72dw130_assertion SIO_000772 19726116 NP447490.RA1poHgfVKXwPScFoV0EfFW1p7U4HdEUsGwpu1vHn72dw130_provenance.
- NP447490.RA1poHgfVKXwPScFoV0EfFW1p7U4HdEUsGwpu1vHn72dw130_assertion wasDerivedFrom befree-20140225 NP447490.RA1poHgfVKXwPScFoV0EfFW1p7U4HdEUsGwpu1vHn72dw130_provenance.
- NP447490.RA1poHgfVKXwPScFoV0EfFW1p7U4HdEUsGwpu1vHn72dw130_assertion wasGeneratedBy ECO_0000203 NP447490.RA1poHgfVKXwPScFoV0EfFW1p7U4HdEUsGwpu1vHn72dw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP447490.RA1poHgfVKXwPScFoV0EfFW1p7U4HdEUsGwpu1vHn72dw130_provenance.