Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP136888.RAdEA45nJ3HK1BCk1r_BbwwNhB0IOFp8LtyAR9xK9rPEQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP136888.RAdEA45nJ3HK1BCk1r_BbwwNhB0IOFp8LtyAR9xK9rPEQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP136888.RAdEA45nJ3HK1BCk1r_BbwwNhB0IOFp8LtyAR9xK9rPEQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP136888.RAdEA45nJ3HK1BCk1r_BbwwNhB0IOFp8LtyAR9xK9rPEQ130_provenance.
- NP136888.RAdEA45nJ3HK1BCk1r_BbwwNhB0IOFp8LtyAR9xK9rPEQ130_assertion description "[The KIAA0319-like (KIAA0319L) gene on chromosome 1p34 as a candidate for reading disabilities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136888.RAdEA45nJ3HK1BCk1r_BbwwNhB0IOFp8LtyAR9xK9rPEQ130_provenance.
- NP136888.RAdEA45nJ3HK1BCk1r_BbwwNhB0IOFp8LtyAR9xK9rPEQ130_assertion evidence source_evidence_literature NP136888.RAdEA45nJ3HK1BCk1r_BbwwNhB0IOFp8LtyAR9xK9rPEQ130_provenance.
- NP136888.RAdEA45nJ3HK1BCk1r_BbwwNhB0IOFp8LtyAR9xK9rPEQ130_assertion SIO_000772 19085271 NP136888.RAdEA45nJ3HK1BCk1r_BbwwNhB0IOFp8LtyAR9xK9rPEQ130_provenance.
- NP136888.RAdEA45nJ3HK1BCk1r_BbwwNhB0IOFp8LtyAR9xK9rPEQ130_assertion wasDerivedFrom gad-20150221 NP136888.RAdEA45nJ3HK1BCk1r_BbwwNhB0IOFp8LtyAR9xK9rPEQ130_provenance.
- NP136888.RAdEA45nJ3HK1BCk1r_BbwwNhB0IOFp8LtyAR9xK9rPEQ130_assertion wasGeneratedBy ECO_0000203 NP136888.RAdEA45nJ3HK1BCk1r_BbwwNhB0IOFp8LtyAR9xK9rPEQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP136888.RAdEA45nJ3HK1BCk1r_BbwwNhB0IOFp8LtyAR9xK9rPEQ130_provenance.