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- source_evidence_literature type ECO_0000212 NP1186492.RAbzOp_S3qdxTM0a1uzBCNeYhzTrva0Di8qY5DSJtZTZA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1186492.RAbzOp_S3qdxTM0a1uzBCNeYhzTrva0Di8qY5DSJtZTZA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1186492.RAbzOp_S3qdxTM0a1uzBCNeYhzTrva0Di8qY5DSJtZTZA130_provenance.
- NP1186492.RAbzOp_S3qdxTM0a1uzBCNeYhzTrva0Di8qY5DSJtZTZA130_assertion description "[We identified 185 infants and children with homozygous or compound heterozygous ABCA3 mutations and lung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1186492.RAbzOp_S3qdxTM0a1uzBCNeYhzTrva0Di8qY5DSJtZTZA130_provenance.
- NP1186492.RAbzOp_S3qdxTM0a1uzBCNeYhzTrva0Di8qY5DSJtZTZA130_assertion evidence source_evidence_literature NP1186492.RAbzOp_S3qdxTM0a1uzBCNeYhzTrva0Di8qY5DSJtZTZA130_provenance.
- NP1186492.RAbzOp_S3qdxTM0a1uzBCNeYhzTrva0Di8qY5DSJtZTZA130_assertion SIO_000772 24871971 NP1186492.RAbzOp_S3qdxTM0a1uzBCNeYhzTrva0Di8qY5DSJtZTZA130_provenance.
- NP1186492.RAbzOp_S3qdxTM0a1uzBCNeYhzTrva0Di8qY5DSJtZTZA130_assertion wasDerivedFrom befree-2016 NP1186492.RAbzOp_S3qdxTM0a1uzBCNeYhzTrva0Di8qY5DSJtZTZA130_provenance.
- NP1186492.RAbzOp_S3qdxTM0a1uzBCNeYhzTrva0Di8qY5DSJtZTZA130_assertion wasGeneratedBy ECO_0000203 NP1186492.RAbzOp_S3qdxTM0a1uzBCNeYhzTrva0Di8qY5DSJtZTZA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1186492.RAbzOp_S3qdxTM0a1uzBCNeYhzTrva0Di8qY5DSJtZTZA130_provenance.