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- NP351744.RAGaqd15P_zlLZdPmJD7UbYraYl2Nehg-n9k1Og-iNq5A130_assertion type Assertion NP351744.RAGaqd15P_zlLZdPmJD7UbYraYl2Nehg-n9k1Og-iNq5A130_head.
- NP351744.RAGaqd15P_zlLZdPmJD7UbYraYl2Nehg-n9k1Og-iNq5A130_assertion wasGeneratedBy ECO_0000203 NP351744.RAGaqd15P_zlLZdPmJD7UbYraYl2Nehg-n9k1Og-iNq5A130_provenance.
- NP351744.RAGaqd15P_zlLZdPmJD7UbYraYl2Nehg-n9k1Og-iNq5A130_assertion wasDerivedFrom befree-2016 NP351744.RAGaqd15P_zlLZdPmJD7UbYraYl2Nehg-n9k1Og-iNq5A130_provenance.
- NP351744.RAGaqd15P_zlLZdPmJD7UbYraYl2Nehg-n9k1Og-iNq5A130_assertion SIO_000772 11951178 NP351744.RAGaqd15P_zlLZdPmJD7UbYraYl2Nehg-n9k1Og-iNq5A130_provenance.
- NP351744.RAGaqd15P_zlLZdPmJD7UbYraYl2Nehg-n9k1Og-iNq5A130_assertion evidence source_evidence_literature NP351744.RAGaqd15P_zlLZdPmJD7UbYraYl2Nehg-n9k1Og-iNq5A130_provenance.
- NP351744.RAGaqd15P_zlLZdPmJD7UbYraYl2Nehg-n9k1Og-iNq5A130_assertion description "[Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351744.RAGaqd15P_zlLZdPmJD7UbYraYl2Nehg-n9k1Og-iNq5A130_provenance.