Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682730.RAalgmZbyeYN3ESu3Rs2mhEreBhYBJdJCwlYQGNCaQ-vw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682730.RAalgmZbyeYN3ESu3Rs2mhEreBhYBJdJCwlYQGNCaQ-vw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682730.RAalgmZbyeYN3ESu3Rs2mhEreBhYBJdJCwlYQGNCaQ-vw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682730.RAalgmZbyeYN3ESu3Rs2mhEreBhYBJdJCwlYQGNCaQ-vw130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP682730.RAalgmZbyeYN3ESu3Rs2mhEreBhYBJdJCwlYQGNCaQ-vw130_provenance.