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- source_evidence_literature type ECO_0000212 NP848675.RADDbjUxNZwRKkHl9dprT7tW36b_j0nwWlgFyrnkl63cU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP848675.RADDbjUxNZwRKkHl9dprT7tW36b_j0nwWlgFyrnkl63cU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP848675.RADDbjUxNZwRKkHl9dprT7tW36b_j0nwWlgFyrnkl63cU130_provenance.
- NP848675.RADDbjUxNZwRKkHl9dprT7tW36b_j0nwWlgFyrnkl63cU130_assertion description "[We tested the hypothesis that a variant of the LIM homeodomain gene LHX4 is responsible for the dwarfism phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP848675.RADDbjUxNZwRKkHl9dprT7tW36b_j0nwWlgFyrnkl63cU130_provenance.
- NP848675.RADDbjUxNZwRKkHl9dprT7tW36b_j0nwWlgFyrnkl63cU130_assertion evidence source_evidence_literature NP848675.RADDbjUxNZwRKkHl9dprT7tW36b_j0nwWlgFyrnkl63cU130_provenance.
- NP848675.RADDbjUxNZwRKkHl9dprT7tW36b_j0nwWlgFyrnkl63cU130_assertion SIO_000772 12431796 NP848675.RADDbjUxNZwRKkHl9dprT7tW36b_j0nwWlgFyrnkl63cU130_provenance.
- NP848675.RADDbjUxNZwRKkHl9dprT7tW36b_j0nwWlgFyrnkl63cU130_assertion wasDerivedFrom befree-20150227 NP848675.RADDbjUxNZwRKkHl9dprT7tW36b_j0nwWlgFyrnkl63cU130_provenance.
- NP848675.RADDbjUxNZwRKkHl9dprT7tW36b_j0nwWlgFyrnkl63cU130_assertion wasGeneratedBy ECO_0000203 NP848675.RADDbjUxNZwRKkHl9dprT7tW36b_j0nwWlgFyrnkl63cU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP848675.RADDbjUxNZwRKkHl9dprT7tW36b_j0nwWlgFyrnkl63cU130_provenance.