Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1023653.RARTq3Izo_j0fUZkiGuarqvP23MbKfCd8U8WlVxi_-YLE130_assertion> ?p ?o ?g. }
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- NP1023653.RARTq3Izo_j0fUZkiGuarqvP23MbKfCd8U8WlVxi_-YLE130_assertion type Assertion NP1023653.RARTq3Izo_j0fUZkiGuarqvP23MbKfCd8U8WlVxi_-YLE130_head.
- NP1023653.RARTq3Izo_j0fUZkiGuarqvP23MbKfCd8U8WlVxi_-YLE130_assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1023653.RARTq3Izo_j0fUZkiGuarqvP23MbKfCd8U8WlVxi_-YLE130_provenance.
- NP1023653.RARTq3Izo_j0fUZkiGuarqvP23MbKfCd8U8WlVxi_-YLE130_assertion evidence source_evidence_literature NP1023653.RARTq3Izo_j0fUZkiGuarqvP23MbKfCd8U8WlVxi_-YLE130_provenance.
- NP1023653.RARTq3Izo_j0fUZkiGuarqvP23MbKfCd8U8WlVxi_-YLE130_assertion SIO_000772 2309698 NP1023653.RARTq3Izo_j0fUZkiGuarqvP23MbKfCd8U8WlVxi_-YLE130_provenance.
- NP1023653.RARTq3Izo_j0fUZkiGuarqvP23MbKfCd8U8WlVxi_-YLE130_assertion wasDerivedFrom befree-2016 NP1023653.RARTq3Izo_j0fUZkiGuarqvP23MbKfCd8U8WlVxi_-YLE130_provenance.
- NP1023653.RARTq3Izo_j0fUZkiGuarqvP23MbKfCd8U8WlVxi_-YLE130_assertion wasGeneratedBy ECO_0000203 NP1023653.RARTq3Izo_j0fUZkiGuarqvP23MbKfCd8U8WlVxi_-YLE130_provenance.