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- source_evidence_literature type ECO_0000212 NP846138.RAaUYe9KhK9GDl-D7_gktAby5O76_pSJbZzx7QKYXUO0Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP846138.RAaUYe9KhK9GDl-D7_gktAby5O76_pSJbZzx7QKYXUO0Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP846138.RAaUYe9KhK9GDl-D7_gktAby5O76_pSJbZzx7QKYXUO0Q130_provenance.
- NP846138.RAaUYe9KhK9GDl-D7_gktAby5O76_pSJbZzx7QKYXUO0Q130_assertion description "[A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP846138.RAaUYe9KhK9GDl-D7_gktAby5O76_pSJbZzx7QKYXUO0Q130_provenance.
- NP846138.RAaUYe9KhK9GDl-D7_gktAby5O76_pSJbZzx7QKYXUO0Q130_assertion evidence source_evidence_literature NP846138.RAaUYe9KhK9GDl-D7_gktAby5O76_pSJbZzx7QKYXUO0Q130_provenance.
- NP846138.RAaUYe9KhK9GDl-D7_gktAby5O76_pSJbZzx7QKYXUO0Q130_assertion SIO_000772 15249611 NP846138.RAaUYe9KhK9GDl-D7_gktAby5O76_pSJbZzx7QKYXUO0Q130_provenance.
- NP846138.RAaUYe9KhK9GDl-D7_gktAby5O76_pSJbZzx7QKYXUO0Q130_assertion wasDerivedFrom befree-20140225 NP846138.RAaUYe9KhK9GDl-D7_gktAby5O76_pSJbZzx7QKYXUO0Q130_provenance.
- NP846138.RAaUYe9KhK9GDl-D7_gktAby5O76_pSJbZzx7QKYXUO0Q130_assertion wasGeneratedBy ECO_0000203 NP846138.RAaUYe9KhK9GDl-D7_gktAby5O76_pSJbZzx7QKYXUO0Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP846138.RAaUYe9KhK9GDl-D7_gktAby5O76_pSJbZzx7QKYXUO0Q130_provenance.