Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP417022.RAdQ7v-_iotcUQXnGEWjiM7-8xZWRfeFj9XWjWyMz5Ajc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP417022.RAdQ7v-_iotcUQXnGEWjiM7-8xZWRfeFj9XWjWyMz5Ajc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP417022.RAdQ7v-_iotcUQXnGEWjiM7-8xZWRfeFj9XWjWyMz5Ajc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP417022.RAdQ7v-_iotcUQXnGEWjiM7-8xZWRfeFj9XWjWyMz5Ajc130_provenance.
- NP417022.RAdQ7v-_iotcUQXnGEWjiM7-8xZWRfeFj9XWjWyMz5Ajc130_assertion description "[Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417022.RAdQ7v-_iotcUQXnGEWjiM7-8xZWRfeFj9XWjWyMz5Ajc130_provenance.
- NP417022.RAdQ7v-_iotcUQXnGEWjiM7-8xZWRfeFj9XWjWyMz5Ajc130_assertion evidence source_evidence_literature NP417022.RAdQ7v-_iotcUQXnGEWjiM7-8xZWRfeFj9XWjWyMz5Ajc130_provenance.
- NP417022.RAdQ7v-_iotcUQXnGEWjiM7-8xZWRfeFj9XWjWyMz5Ajc130_assertion SIO_000772 17215107 NP417022.RAdQ7v-_iotcUQXnGEWjiM7-8xZWRfeFj9XWjWyMz5Ajc130_provenance.
- NP417022.RAdQ7v-_iotcUQXnGEWjiM7-8xZWRfeFj9XWjWyMz5Ajc130_assertion wasDerivedFrom befree-20150227 NP417022.RAdQ7v-_iotcUQXnGEWjiM7-8xZWRfeFj9XWjWyMz5Ajc130_provenance.
- NP417022.RAdQ7v-_iotcUQXnGEWjiM7-8xZWRfeFj9XWjWyMz5Ajc130_assertion wasGeneratedBy ECO_0000203 NP417022.RAdQ7v-_iotcUQXnGEWjiM7-8xZWRfeFj9XWjWyMz5Ajc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP417022.RAdQ7v-_iotcUQXnGEWjiM7-8xZWRfeFj9XWjWyMz5Ajc130_provenance.