Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP151946.RAdHHOFbvN9XljtcQp25CC7HKfAnq7DlLg2xW-ONuSlLQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP151946.RAdHHOFbvN9XljtcQp25CC7HKfAnq7DlLg2xW-ONuSlLQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP151946.RAdHHOFbvN9XljtcQp25CC7HKfAnq7DlLg2xW-ONuSlLQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP151946.RAdHHOFbvN9XljtcQp25CC7HKfAnq7DlLg2xW-ONuSlLQ130_provenance.
- NP151946.RAdHHOFbvN9XljtcQp25CC7HKfAnq7DlLg2xW-ONuSlLQ130_assertion description "[novel nonsense mutations in 2 African American siblings with autosomal recessive Alport syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP151946.RAdHHOFbvN9XljtcQp25CC7HKfAnq7DlLg2xW-ONuSlLQ130_provenance.
- NP151946.RAdHHOFbvN9XljtcQp25CC7HKfAnq7DlLg2xW-ONuSlLQ130_assertion evidence source_evidence_literature NP151946.RAdHHOFbvN9XljtcQp25CC7HKfAnq7DlLg2xW-ONuSlLQ130_provenance.
- NP151946.RAdHHOFbvN9XljtcQp25CC7HKfAnq7DlLg2xW-ONuSlLQ130_assertion SIO_000772 18436078 NP151946.RAdHHOFbvN9XljtcQp25CC7HKfAnq7DlLg2xW-ONuSlLQ130_provenance.
- NP151946.RAdHHOFbvN9XljtcQp25CC7HKfAnq7DlLg2xW-ONuSlLQ130_assertion wasDerivedFrom lhgdn-20090331 NP151946.RAdHHOFbvN9XljtcQp25CC7HKfAnq7DlLg2xW-ONuSlLQ130_provenance.
- NP151946.RAdHHOFbvN9XljtcQp25CC7HKfAnq7DlLg2xW-ONuSlLQ130_assertion wasGeneratedBy ECO_0000203 NP151946.RAdHHOFbvN9XljtcQp25CC7HKfAnq7DlLg2xW-ONuSlLQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP151946.RAdHHOFbvN9XljtcQp25CC7HKfAnq7DlLg2xW-ONuSlLQ130_provenance.