Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP145241.RAonCIQs4KnPTwwNGysrDqM1YmPRaIbMFcx7C6_vOrZCg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP145241.RAonCIQs4KnPTwwNGysrDqM1YmPRaIbMFcx7C6_vOrZCg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP145241.RAonCIQs4KnPTwwNGysrDqM1YmPRaIbMFcx7C6_vOrZCg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP145241.RAonCIQs4KnPTwwNGysrDqM1YmPRaIbMFcx7C6_vOrZCg130_provenance.
- NP145241.RAonCIQs4KnPTwwNGysrDqM1YmPRaIbMFcx7C6_vOrZCg130_assertion description "[Ardalan-Shoja-Kiuru syndrome, a hereditary gelsolin amyloidosis plus retinitis pigmentosa, is due to a G654A gelsolin mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145241.RAonCIQs4KnPTwwNGysrDqM1YmPRaIbMFcx7C6_vOrZCg130_provenance.
- NP145241.RAonCIQs4KnPTwwNGysrDqM1YmPRaIbMFcx7C6_vOrZCg130_assertion evidence source_evidence_literature NP145241.RAonCIQs4KnPTwwNGysrDqM1YmPRaIbMFcx7C6_vOrZCg130_provenance.
- NP145241.RAonCIQs4KnPTwwNGysrDqM1YmPRaIbMFcx7C6_vOrZCg130_assertion SIO_000772 17720986 NP145241.RAonCIQs4KnPTwwNGysrDqM1YmPRaIbMFcx7C6_vOrZCg130_provenance.
- NP145241.RAonCIQs4KnPTwwNGysrDqM1YmPRaIbMFcx7C6_vOrZCg130_assertion wasDerivedFrom lhgdn-20090331 NP145241.RAonCIQs4KnPTwwNGysrDqM1YmPRaIbMFcx7C6_vOrZCg130_provenance.
- NP145241.RAonCIQs4KnPTwwNGysrDqM1YmPRaIbMFcx7C6_vOrZCg130_assertion wasGeneratedBy ECO_0000203 NP145241.RAonCIQs4KnPTwwNGysrDqM1YmPRaIbMFcx7C6_vOrZCg130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP145241.RAonCIQs4KnPTwwNGysrDqM1YmPRaIbMFcx7C6_vOrZCg130_provenance.