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- source_evidence_literature type ECO_0000212 NP1023652.RAmKRN1F1m6SHovpkWXHv3k-ySm0GhRutuyajI8nBOkrU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1023652.RAmKRN1F1m6SHovpkWXHv3k-ySm0GhRutuyajI8nBOkrU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1023652.RAmKRN1F1m6SHovpkWXHv3k-ySm0GhRutuyajI8nBOkrU130_provenance.
- NP1023652.RAmKRN1F1m6SHovpkWXHv3k-ySm0GhRutuyajI8nBOkrU130_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." NP1023652.RAmKRN1F1m6SHovpkWXHv3k-ySm0GhRutuyajI8nBOkrU130_provenance.
- NP1023652.RAmKRN1F1m6SHovpkWXHv3k-ySm0GhRutuyajI8nBOkrU130_assertion evidence source_evidence_literature NP1023652.RAmKRN1F1m6SHovpkWXHv3k-ySm0GhRutuyajI8nBOkrU130_provenance.
- NP1023652.RAmKRN1F1m6SHovpkWXHv3k-ySm0GhRutuyajI8nBOkrU130_assertion SIO_000772 2309698 NP1023652.RAmKRN1F1m6SHovpkWXHv3k-ySm0GhRutuyajI8nBOkrU130_provenance.
- NP1023652.RAmKRN1F1m6SHovpkWXHv3k-ySm0GhRutuyajI8nBOkrU130_assertion wasDerivedFrom befree-2016 NP1023652.RAmKRN1F1m6SHovpkWXHv3k-ySm0GhRutuyajI8nBOkrU130_provenance.
- NP1023652.RAmKRN1F1m6SHovpkWXHv3k-ySm0GhRutuyajI8nBOkrU130_assertion wasGeneratedBy ECO_0000203 NP1023652.RAmKRN1F1m6SHovpkWXHv3k-ySm0GhRutuyajI8nBOkrU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1023652.RAmKRN1F1m6SHovpkWXHv3k-ySm0GhRutuyajI8nBOkrU130_provenance.