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- source_evidence_literature type ECO_0000212 NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_provenance.
- NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_assertion description "[Allelic association of a truncation mutation of the KCNMB3 gene with idiopathic generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_provenance.
- NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_assertion evidence source_evidence_literature NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_provenance.
- NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_assertion SIO_000772 16958040 NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_provenance.
- NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_assertion wasDerivedFrom befree-2016 NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_provenance.
- NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_assertion wasGeneratedBy ECO_0000203 NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_provenance.
- befree-2016 importedOn "2016-02-19" NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_provenance.