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- source_evidence_literature type ECO_0000212 NP524146.RAXqpMMlU_14oHxWPkc738hriEml0tdGlIK0K8xYXmy2A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP524146.RAXqpMMlU_14oHxWPkc738hriEml0tdGlIK0K8xYXmy2A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP524146.RAXqpMMlU_14oHxWPkc738hriEml0tdGlIK0K8xYXmy2A130_provenance.
- NP524146.RAXqpMMlU_14oHxWPkc738hriEml0tdGlIK0K8xYXmy2A130_assertion description "[Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP524146.RAXqpMMlU_14oHxWPkc738hriEml0tdGlIK0K8xYXmy2A130_provenance.
- NP524146.RAXqpMMlU_14oHxWPkc738hriEml0tdGlIK0K8xYXmy2A130_assertion evidence source_evidence_literature NP524146.RAXqpMMlU_14oHxWPkc738hriEml0tdGlIK0K8xYXmy2A130_provenance.
- NP524146.RAXqpMMlU_14oHxWPkc738hriEml0tdGlIK0K8xYXmy2A130_assertion SIO_000772 23603762 NP524146.RAXqpMMlU_14oHxWPkc738hriEml0tdGlIK0K8xYXmy2A130_provenance.
- NP524146.RAXqpMMlU_14oHxWPkc738hriEml0tdGlIK0K8xYXmy2A130_assertion wasDerivedFrom befree-20150227 NP524146.RAXqpMMlU_14oHxWPkc738hriEml0tdGlIK0K8xYXmy2A130_provenance.
- NP524146.RAXqpMMlU_14oHxWPkc738hriEml0tdGlIK0K8xYXmy2A130_assertion wasGeneratedBy ECO_0000203 NP524146.RAXqpMMlU_14oHxWPkc738hriEml0tdGlIK0K8xYXmy2A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP524146.RAXqpMMlU_14oHxWPkc738hriEml0tdGlIK0K8xYXmy2A130_provenance.