Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP394388.RAwOktpIL2-9PrRFg-9jTVjchaaKgNDH_9s0rmjL_mVew130_assertion> ?p ?o ?g. }
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- NP394388.RAwOktpIL2-9PrRFg-9jTVjchaaKgNDH_9s0rmjL_mVew130_assertion type Assertion NP394388.RAwOktpIL2-9PrRFg-9jTVjchaaKgNDH_9s0rmjL_mVew130_head.
- NP394388.RAwOktpIL2-9PrRFg-9jTVjchaaKgNDH_9s0rmjL_mVew130_assertion description "[DYX1C1: was recently identified as a candidate gene for developmental dyslexia, which is characterized by an unexpected difficulty in learning to read and write despite adequate intelligence, motivation, and education.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP394388.RAwOktpIL2-9PrRFg-9jTVjchaaKgNDH_9s0rmjL_mVew130_provenance.
- NP394388.RAwOktpIL2-9PrRFg-9jTVjchaaKgNDH_9s0rmjL_mVew130_assertion evidence source_evidence_literature NP394388.RAwOktpIL2-9PrRFg-9jTVjchaaKgNDH_9s0rmjL_mVew130_provenance.
- NP394388.RAwOktpIL2-9PrRFg-9jTVjchaaKgNDH_9s0rmjL_mVew130_assertion SIO_000772 15470369 NP394388.RAwOktpIL2-9PrRFg-9jTVjchaaKgNDH_9s0rmjL_mVew130_provenance.
- NP394388.RAwOktpIL2-9PrRFg-9jTVjchaaKgNDH_9s0rmjL_mVew130_assertion wasDerivedFrom befree-20140225 NP394388.RAwOktpIL2-9PrRFg-9jTVjchaaKgNDH_9s0rmjL_mVew130_provenance.
- NP394388.RAwOktpIL2-9PrRFg-9jTVjchaaKgNDH_9s0rmjL_mVew130_assertion wasGeneratedBy ECO_0000203 NP394388.RAwOktpIL2-9PrRFg-9jTVjchaaKgNDH_9s0rmjL_mVew130_provenance.