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- source_evidence_literature type ECO_0000212 NP490195.RAfDTHfjAkZQDq5RE0_1qwzvNF5UFeepB1Y5ycWEw7u4A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP490195.RAfDTHfjAkZQDq5RE0_1qwzvNF5UFeepB1Y5ycWEw7u4A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP490195.RAfDTHfjAkZQDq5RE0_1qwzvNF5UFeepB1Y5ycWEw7u4A130_provenance.
- NP490195.RAfDTHfjAkZQDq5RE0_1qwzvNF5UFeepB1Y5ycWEw7u4A130_assertion description "[Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490195.RAfDTHfjAkZQDq5RE0_1qwzvNF5UFeepB1Y5ycWEw7u4A130_provenance.
- NP490195.RAfDTHfjAkZQDq5RE0_1qwzvNF5UFeepB1Y5ycWEw7u4A130_assertion evidence source_evidence_literature NP490195.RAfDTHfjAkZQDq5RE0_1qwzvNF5UFeepB1Y5ycWEw7u4A130_provenance.
- NP490195.RAfDTHfjAkZQDq5RE0_1qwzvNF5UFeepB1Y5ycWEw7u4A130_assertion SIO_000772 15833430 NP490195.RAfDTHfjAkZQDq5RE0_1qwzvNF5UFeepB1Y5ycWEw7u4A130_provenance.
- NP490195.RAfDTHfjAkZQDq5RE0_1qwzvNF5UFeepB1Y5ycWEw7u4A130_assertion wasDerivedFrom befree-2016 NP490195.RAfDTHfjAkZQDq5RE0_1qwzvNF5UFeepB1Y5ycWEw7u4A130_provenance.
- NP490195.RAfDTHfjAkZQDq5RE0_1qwzvNF5UFeepB1Y5ycWEw7u4A130_assertion wasGeneratedBy ECO_0000203 NP490195.RAfDTHfjAkZQDq5RE0_1qwzvNF5UFeepB1Y5ycWEw7u4A130_provenance.
- befree-2016 importedOn "2016-02-19" NP490195.RAfDTHfjAkZQDq5RE0_1qwzvNF5UFeepB1Y5ycWEw7u4A130_provenance.