Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP350038.RAQSsqBmniD24FU8xQx02cRv7BAQCHGoNDcK4wvLZD3lE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP350038.RAQSsqBmniD24FU8xQx02cRv7BAQCHGoNDcK4wvLZD3lE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP350038.RAQSsqBmniD24FU8xQx02cRv7BAQCHGoNDcK4wvLZD3lE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP350038.RAQSsqBmniD24FU8xQx02cRv7BAQCHGoNDcK4wvLZD3lE130_provenance.
- NP350038.RAQSsqBmniD24FU8xQx02cRv7BAQCHGoNDcK4wvLZD3lE130_assertion description "[Sequencing of the GRIK1 gene in patients with juvenile absence epilepsy does not reveal mutations affecting receptor structure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP350038.RAQSsqBmniD24FU8xQx02cRv7BAQCHGoNDcK4wvLZD3lE130_provenance.
- NP350038.RAQSsqBmniD24FU8xQx02cRv7BAQCHGoNDcK4wvLZD3lE130_assertion evidence source_evidence_literature NP350038.RAQSsqBmniD24FU8xQx02cRv7BAQCHGoNDcK4wvLZD3lE130_provenance.
- NP350038.RAQSsqBmniD24FU8xQx02cRv7BAQCHGoNDcK4wvLZD3lE130_assertion SIO_000772 11920863 NP350038.RAQSsqBmniD24FU8xQx02cRv7BAQCHGoNDcK4wvLZD3lE130_provenance.
- NP350038.RAQSsqBmniD24FU8xQx02cRv7BAQCHGoNDcK4wvLZD3lE130_assertion wasDerivedFrom befree-2016 NP350038.RAQSsqBmniD24FU8xQx02cRv7BAQCHGoNDcK4wvLZD3lE130_provenance.
- NP350038.RAQSsqBmniD24FU8xQx02cRv7BAQCHGoNDcK4wvLZD3lE130_assertion wasGeneratedBy ECO_0000203 NP350038.RAQSsqBmniD24FU8xQx02cRv7BAQCHGoNDcK4wvLZD3lE130_provenance.
- befree-2016 importedOn "2016-02-19" NP350038.RAQSsqBmniD24FU8xQx02cRv7BAQCHGoNDcK4wvLZD3lE130_provenance.