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- source_evidence_literature type ECO_0000212 NP801288.RAXp3LesdWRIciKAcSb1_ovPqfF2kdCJ3HaEUZYG3LOIA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP801288.RAXp3LesdWRIciKAcSb1_ovPqfF2kdCJ3HaEUZYG3LOIA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP801288.RAXp3LesdWRIciKAcSb1_ovPqfF2kdCJ3HaEUZYG3LOIA130_provenance.
- NP801288.RAXp3LesdWRIciKAcSb1_ovPqfF2kdCJ3HaEUZYG3LOIA130_assertion description "[We review cases with cytogenetic anomalies involving 8p23.1, discuss a potential relationship between 8p23.1 deletions and CdLS and suggest a novel candidate gene for CdLS-Tankyrase 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801288.RAXp3LesdWRIciKAcSb1_ovPqfF2kdCJ3HaEUZYG3LOIA130_provenance.
- NP801288.RAXp3LesdWRIciKAcSb1_ovPqfF2kdCJ3HaEUZYG3LOIA130_assertion evidence source_evidence_literature NP801288.RAXp3LesdWRIciKAcSb1_ovPqfF2kdCJ3HaEUZYG3LOIA130_provenance.
- NP801288.RAXp3LesdWRIciKAcSb1_ovPqfF2kdCJ3HaEUZYG3LOIA130_assertion SIO_000772 18470924 NP801288.RAXp3LesdWRIciKAcSb1_ovPqfF2kdCJ3HaEUZYG3LOIA130_provenance.
- NP801288.RAXp3LesdWRIciKAcSb1_ovPqfF2kdCJ3HaEUZYG3LOIA130_assertion wasDerivedFrom befree-20150227 NP801288.RAXp3LesdWRIciKAcSb1_ovPqfF2kdCJ3HaEUZYG3LOIA130_provenance.
- NP801288.RAXp3LesdWRIciKAcSb1_ovPqfF2kdCJ3HaEUZYG3LOIA130_assertion wasGeneratedBy ECO_0000203 NP801288.RAXp3LesdWRIciKAcSb1_ovPqfF2kdCJ3HaEUZYG3LOIA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP801288.RAXp3LesdWRIciKAcSb1_ovPqfF2kdCJ3HaEUZYG3LOIA130_provenance.