Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP682730.RAalgmZbyeYN3ESu3Rs2mhEreBhYBJdJCwlYQGNCaQ-vw130_assertion> ?p ?o ?g. }
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- NP682730.RAalgmZbyeYN3ESu3Rs2mhEreBhYBJdJCwlYQGNCaQ-vw130_assertion type Assertion NP682730.RAalgmZbyeYN3ESu3Rs2mhEreBhYBJdJCwlYQGNCaQ-vw130_head.
- NP682730.RAalgmZbyeYN3ESu3Rs2mhEreBhYBJdJCwlYQGNCaQ-vw130_assertion description "[Compromised function in the Na(v)1.2 Dravet syndrome mutation R1312T.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682730.RAalgmZbyeYN3ESu3Rs2mhEreBhYBJdJCwlYQGNCaQ-vw130_provenance.
- NP682730.RAalgmZbyeYN3ESu3Rs2mhEreBhYBJdJCwlYQGNCaQ-vw130_assertion evidence source_evidence_literature NP682730.RAalgmZbyeYN3ESu3Rs2mhEreBhYBJdJCwlYQGNCaQ-vw130_provenance.
- NP682730.RAalgmZbyeYN3ESu3Rs2mhEreBhYBJdJCwlYQGNCaQ-vw130_assertion SIO_000772 22677033 NP682730.RAalgmZbyeYN3ESu3Rs2mhEreBhYBJdJCwlYQGNCaQ-vw130_provenance.
- NP682730.RAalgmZbyeYN3ESu3Rs2mhEreBhYBJdJCwlYQGNCaQ-vw130_assertion wasDerivedFrom befree-20150227 NP682730.RAalgmZbyeYN3ESu3Rs2mhEreBhYBJdJCwlYQGNCaQ-vw130_provenance.
- NP682730.RAalgmZbyeYN3ESu3Rs2mhEreBhYBJdJCwlYQGNCaQ-vw130_assertion wasGeneratedBy ECO_0000203 NP682730.RAalgmZbyeYN3ESu3Rs2mhEreBhYBJdJCwlYQGNCaQ-vw130_provenance.