Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP495138.RAndoPqTBJ2E1Ch0Y7-0x6y8m_qanHFPbPP3i_VLBcahc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP495138.RAndoPqTBJ2E1Ch0Y7-0x6y8m_qanHFPbPP3i_VLBcahc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP495138.RAndoPqTBJ2E1Ch0Y7-0x6y8m_qanHFPbPP3i_VLBcahc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP495138.RAndoPqTBJ2E1Ch0Y7-0x6y8m_qanHFPbPP3i_VLBcahc130_provenance.
- NP495138.RAndoPqTBJ2E1Ch0Y7-0x6y8m_qanHFPbPP3i_VLBcahc130_assertion wasGeneratedBy ECO_0000203 NP495138.RAndoPqTBJ2E1Ch0Y7-0x6y8m_qanHFPbPP3i_VLBcahc130_provenance.
- NP495138.RAndoPqTBJ2E1Ch0Y7-0x6y8m_qanHFPbPP3i_VLBcahc130_assertion wasDerivedFrom befree-20140225 NP495138.RAndoPqTBJ2E1Ch0Y7-0x6y8m_qanHFPbPP3i_VLBcahc130_provenance.
- NP495138.RAndoPqTBJ2E1Ch0Y7-0x6y8m_qanHFPbPP3i_VLBcahc130_assertion SIO_000772 12771268 NP495138.RAndoPqTBJ2E1Ch0Y7-0x6y8m_qanHFPbPP3i_VLBcahc130_provenance.
- NP495138.RAndoPqTBJ2E1Ch0Y7-0x6y8m_qanHFPbPP3i_VLBcahc130_assertion evidence source_evidence_literature NP495138.RAndoPqTBJ2E1Ch0Y7-0x6y8m_qanHFPbPP3i_VLBcahc130_provenance.
- NP495138.RAndoPqTBJ2E1Ch0Y7-0x6y8m_qanHFPbPP3i_VLBcahc130_assertion description "[Novel LGI1 mutation in a family with autosomal dominant partial epilepsy with auditory features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP495138.RAndoPqTBJ2E1Ch0Y7-0x6y8m_qanHFPbPP3i_VLBcahc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP495138.RAndoPqTBJ2E1Ch0Y7-0x6y8m_qanHFPbPP3i_VLBcahc130_provenance.