Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP593331.RAIh61g5LmT3vP7zSpPRt8SVMooJwMpwPAMIygWEHkwZs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP593331.RAIh61g5LmT3vP7zSpPRt8SVMooJwMpwPAMIygWEHkwZs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP593331.RAIh61g5LmT3vP7zSpPRt8SVMooJwMpwPAMIygWEHkwZs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP593331.RAIh61g5LmT3vP7zSpPRt8SVMooJwMpwPAMIygWEHkwZs130_provenance.
- NP593331.RAIh61g5LmT3vP7zSpPRt8SVMooJwMpwPAMIygWEHkwZs130_assertion description "[Although L1CAM is expressed during renal development and L1cam-deficient mice have congenital malformations of the kidney and the urinary tract, L1CAM mutations have not been associated with renal anomalies in men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593331.RAIh61g5LmT3vP7zSpPRt8SVMooJwMpwPAMIygWEHkwZs130_provenance.
- NP593331.RAIh61g5LmT3vP7zSpPRt8SVMooJwMpwPAMIygWEHkwZs130_assertion evidence source_evidence_literature NP593331.RAIh61g5LmT3vP7zSpPRt8SVMooJwMpwPAMIygWEHkwZs130_provenance.
- NP593331.RAIh61g5LmT3vP7zSpPRt8SVMooJwMpwPAMIygWEHkwZs130_assertion SIO_000772 17294222 NP593331.RAIh61g5LmT3vP7zSpPRt8SVMooJwMpwPAMIygWEHkwZs130_provenance.
- NP593331.RAIh61g5LmT3vP7zSpPRt8SVMooJwMpwPAMIygWEHkwZs130_assertion wasDerivedFrom befree-2016 NP593331.RAIh61g5LmT3vP7zSpPRt8SVMooJwMpwPAMIygWEHkwZs130_provenance.
- NP593331.RAIh61g5LmT3vP7zSpPRt8SVMooJwMpwPAMIygWEHkwZs130_assertion wasGeneratedBy ECO_0000203 NP593331.RAIh61g5LmT3vP7zSpPRt8SVMooJwMpwPAMIygWEHkwZs130_provenance.
- befree-2016 importedOn "2016-02-19" NP593331.RAIh61g5LmT3vP7zSpPRt8SVMooJwMpwPAMIygWEHkwZs130_provenance.