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- source_evidence_literature type ECO_0000212 NP355795.RArlT2CeIlL-uhzn5jIZ1JbS5HMfCg7uBFjO6QIohMvPI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP355795.RArlT2CeIlL-uhzn5jIZ1JbS5HMfCg7uBFjO6QIohMvPI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP355795.RArlT2CeIlL-uhzn5jIZ1JbS5HMfCg7uBFjO6QIohMvPI130_provenance.
- NP355795.RArlT2CeIlL-uhzn5jIZ1JbS5HMfCg7uBFjO6QIohMvPI130_assertion description "[Sporadic patients who had tested negative for COL4A5 mutations were included with typical cases of autosomal recessive ATS to secure a better definition of the phenotype spectrum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355795.RArlT2CeIlL-uhzn5jIZ1JbS5HMfCg7uBFjO6QIohMvPI130_provenance.
- NP355795.RArlT2CeIlL-uhzn5jIZ1JbS5HMfCg7uBFjO6QIohMvPI130_assertion evidence source_evidence_literature NP355795.RArlT2CeIlL-uhzn5jIZ1JbS5HMfCg7uBFjO6QIohMvPI130_provenance.
- NP355795.RArlT2CeIlL-uhzn5jIZ1JbS5HMfCg7uBFjO6QIohMvPI130_assertion SIO_000772 12028435 NP355795.RArlT2CeIlL-uhzn5jIZ1JbS5HMfCg7uBFjO6QIohMvPI130_provenance.
- NP355795.RArlT2CeIlL-uhzn5jIZ1JbS5HMfCg7uBFjO6QIohMvPI130_assertion wasDerivedFrom befree-2016 NP355795.RArlT2CeIlL-uhzn5jIZ1JbS5HMfCg7uBFjO6QIohMvPI130_provenance.
- NP355795.RArlT2CeIlL-uhzn5jIZ1JbS5HMfCg7uBFjO6QIohMvPI130_assertion wasGeneratedBy ECO_0000203 NP355795.RArlT2CeIlL-uhzn5jIZ1JbS5HMfCg7uBFjO6QIohMvPI130_provenance.
- befree-2016 importedOn "2016-02-19" NP355795.RArlT2CeIlL-uhzn5jIZ1JbS5HMfCg7uBFjO6QIohMvPI130_provenance.