Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682553.RA0wCR6dN6J_Pfvup7l_DpCCtdKBPXVnbUxRMzOZp9cPY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682553.RA0wCR6dN6J_Pfvup7l_DpCCtdKBPXVnbUxRMzOZp9cPY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682553.RA0wCR6dN6J_Pfvup7l_DpCCtdKBPXVnbUxRMzOZp9cPY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682553.RA0wCR6dN6J_Pfvup7l_DpCCtdKBPXVnbUxRMzOZp9cPY130_provenance.
- NP682553.RA0wCR6dN6J_Pfvup7l_DpCCtdKBPXVnbUxRMzOZp9cPY130_assertion description "[The clinical features of severe myoclonic epilepsy of infancy (SMEI) resemble those of mitochondrial diseases, although most patients have the sodium channel (SCN1A) mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682553.RA0wCR6dN6J_Pfvup7l_DpCCtdKBPXVnbUxRMzOZp9cPY130_provenance.
- NP682553.RA0wCR6dN6J_Pfvup7l_DpCCtdKBPXVnbUxRMzOZp9cPY130_assertion evidence source_evidence_literature NP682553.RA0wCR6dN6J_Pfvup7l_DpCCtdKBPXVnbUxRMzOZp9cPY130_provenance.
- NP682553.RA0wCR6dN6J_Pfvup7l_DpCCtdKBPXVnbUxRMzOZp9cPY130_assertion SIO_000772 19359143 NP682553.RA0wCR6dN6J_Pfvup7l_DpCCtdKBPXVnbUxRMzOZp9cPY130_provenance.
- NP682553.RA0wCR6dN6J_Pfvup7l_DpCCtdKBPXVnbUxRMzOZp9cPY130_assertion wasDerivedFrom befree-20150227 NP682553.RA0wCR6dN6J_Pfvup7l_DpCCtdKBPXVnbUxRMzOZp9cPY130_provenance.
- NP682553.RA0wCR6dN6J_Pfvup7l_DpCCtdKBPXVnbUxRMzOZp9cPY130_assertion wasGeneratedBy ECO_0000203 NP682553.RA0wCR6dN6J_Pfvup7l_DpCCtdKBPXVnbUxRMzOZp9cPY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP682553.RA0wCR6dN6J_Pfvup7l_DpCCtdKBPXVnbUxRMzOZp9cPY130_provenance.