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- source_evidence_literature type ECO_0000212 NP374331.RAP8hfRDrTWScwvupT45-NempEoAZ_yDEOoUdOvQn5ijA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP374331.RAP8hfRDrTWScwvupT45-NempEoAZ_yDEOoUdOvQn5ijA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP374331.RAP8hfRDrTWScwvupT45-NempEoAZ_yDEOoUdOvQn5ijA130_provenance.
- NP374331.RAP8hfRDrTWScwvupT45-NempEoAZ_yDEOoUdOvQn5ijA130_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." NP374331.RAP8hfRDrTWScwvupT45-NempEoAZ_yDEOoUdOvQn5ijA130_provenance.
- NP374331.RAP8hfRDrTWScwvupT45-NempEoAZ_yDEOoUdOvQn5ijA130_assertion evidence source_evidence_literature NP374331.RAP8hfRDrTWScwvupT45-NempEoAZ_yDEOoUdOvQn5ijA130_provenance.
- NP374331.RAP8hfRDrTWScwvupT45-NempEoAZ_yDEOoUdOvQn5ijA130_assertion SIO_000772 12431796 NP374331.RAP8hfRDrTWScwvupT45-NempEoAZ_yDEOoUdOvQn5ijA130_provenance.
- NP374331.RAP8hfRDrTWScwvupT45-NempEoAZ_yDEOoUdOvQn5ijA130_assertion wasDerivedFrom befree-2016 NP374331.RAP8hfRDrTWScwvupT45-NempEoAZ_yDEOoUdOvQn5ijA130_provenance.
- NP374331.RAP8hfRDrTWScwvupT45-NempEoAZ_yDEOoUdOvQn5ijA130_assertion wasGeneratedBy ECO_0000203 NP374331.RAP8hfRDrTWScwvupT45-NempEoAZ_yDEOoUdOvQn5ijA130_provenance.
- befree-2016 importedOn "2016-02-19" NP374331.RAP8hfRDrTWScwvupT45-NempEoAZ_yDEOoUdOvQn5ijA130_provenance.