Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP358813.RAQ1Rmz41d83mljm8hKsf_Or5nb4CyNoDhW1d-Dsqx__s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP358813.RAQ1Rmz41d83mljm8hKsf_Or5nb4CyNoDhW1d-Dsqx__s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP358813.RAQ1Rmz41d83mljm8hKsf_Or5nb4CyNoDhW1d-Dsqx__s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP358813.RAQ1Rmz41d83mljm8hKsf_Or5nb4CyNoDhW1d-Dsqx__s130_provenance.
- NP358813.RAQ1Rmz41d83mljm8hKsf_Or5nb4CyNoDhW1d-Dsqx__s130_assertion wasGeneratedBy ECO_0000203 NP358813.RAQ1Rmz41d83mljm8hKsf_Or5nb4CyNoDhW1d-Dsqx__s130_provenance.
- NP358813.RAQ1Rmz41d83mljm8hKsf_Or5nb4CyNoDhW1d-Dsqx__s130_assertion wasDerivedFrom befree-20140225 NP358813.RAQ1Rmz41d83mljm8hKsf_Or5nb4CyNoDhW1d-Dsqx__s130_provenance.
- NP358813.RAQ1Rmz41d83mljm8hKsf_Or5nb4CyNoDhW1d-Dsqx__s130_assertion SIO_000772 23438977 NP358813.RAQ1Rmz41d83mljm8hKsf_Or5nb4CyNoDhW1d-Dsqx__s130_provenance.
- NP358813.RAQ1Rmz41d83mljm8hKsf_Or5nb4CyNoDhW1d-Dsqx__s130_assertion evidence source_evidence_literature NP358813.RAQ1Rmz41d83mljm8hKsf_Or5nb4CyNoDhW1d-Dsqx__s130_provenance.
- NP358813.RAQ1Rmz41d83mljm8hKsf_Or5nb4CyNoDhW1d-Dsqx__s130_assertion description "[Transthyretin Ala36Pro mutation in a Chinese pedigree of familial transthyretin amyloidosis with elevated vitreous and serum vascular endothelial growth factor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358813.RAQ1Rmz41d83mljm8hKsf_Or5nb4CyNoDhW1d-Dsqx__s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP358813.RAQ1Rmz41d83mljm8hKsf_Or5nb4CyNoDhW1d-Dsqx__s130_provenance.