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- source_evidence_literature type ECO_0000212 NP600520.RAl-oKl8WAzG-6mijiqUeC_f4pOCD2UzLmQw4ioCFGUlY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP600520.RAl-oKl8WAzG-6mijiqUeC_f4pOCD2UzLmQw4ioCFGUlY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP600520.RAl-oKl8WAzG-6mijiqUeC_f4pOCD2UzLmQw4ioCFGUlY130_provenance.
- NP600520.RAl-oKl8WAzG-6mijiqUeC_f4pOCD2UzLmQw4ioCFGUlY130_assertion description "[Identification of a novel causative mutation in the ROR2 gene in a Lebanese family with a mild form of recessive Robinow syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600520.RAl-oKl8WAzG-6mijiqUeC_f4pOCD2UzLmQw4ioCFGUlY130_provenance.
- NP600520.RAl-oKl8WAzG-6mijiqUeC_f4pOCD2UzLmQw4ioCFGUlY130_assertion evidence source_evidence_literature NP600520.RAl-oKl8WAzG-6mijiqUeC_f4pOCD2UzLmQw4ioCFGUlY130_provenance.
- NP600520.RAl-oKl8WAzG-6mijiqUeC_f4pOCD2UzLmQw4ioCFGUlY130_assertion SIO_000772 22178368 NP600520.RAl-oKl8WAzG-6mijiqUeC_f4pOCD2UzLmQw4ioCFGUlY130_provenance.
- NP600520.RAl-oKl8WAzG-6mijiqUeC_f4pOCD2UzLmQw4ioCFGUlY130_assertion wasDerivedFrom befree-20150227 NP600520.RAl-oKl8WAzG-6mijiqUeC_f4pOCD2UzLmQw4ioCFGUlY130_provenance.
- NP600520.RAl-oKl8WAzG-6mijiqUeC_f4pOCD2UzLmQw4ioCFGUlY130_assertion wasGeneratedBy ECO_0000203 NP600520.RAl-oKl8WAzG-6mijiqUeC_f4pOCD2UzLmQw4ioCFGUlY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP600520.RAl-oKl8WAzG-6mijiqUeC_f4pOCD2UzLmQw4ioCFGUlY130_provenance.