Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP357579.RAxx8lWiTKNZppE3wKfm89TS79aRJbABP1rhBBBQt_2K0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP357579.RAxx8lWiTKNZppE3wKfm89TS79aRJbABP1rhBBBQt_2K0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP357579.RAxx8lWiTKNZppE3wKfm89TS79aRJbABP1rhBBBQt_2K0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP357579.RAxx8lWiTKNZppE3wKfm89TS79aRJbABP1rhBBBQt_2K0130_provenance.
- NP357579.RAxx8lWiTKNZppE3wKfm89TS79aRJbABP1rhBBBQt_2K0130_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." NP357579.RAxx8lWiTKNZppE3wKfm89TS79aRJbABP1rhBBBQt_2K0130_provenance.
- NP357579.RAxx8lWiTKNZppE3wKfm89TS79aRJbABP1rhBBBQt_2K0130_assertion evidence source_evidence_literature NP357579.RAxx8lWiTKNZppE3wKfm89TS79aRJbABP1rhBBBQt_2K0130_provenance.
- NP357579.RAxx8lWiTKNZppE3wKfm89TS79aRJbABP1rhBBBQt_2K0130_assertion SIO_000772 2309698 NP357579.RAxx8lWiTKNZppE3wKfm89TS79aRJbABP1rhBBBQt_2K0130_provenance.
- NP357579.RAxx8lWiTKNZppE3wKfm89TS79aRJbABP1rhBBBQt_2K0130_assertion wasDerivedFrom befree-20140225 NP357579.RAxx8lWiTKNZppE3wKfm89TS79aRJbABP1rhBBBQt_2K0130_provenance.
- NP357579.RAxx8lWiTKNZppE3wKfm89TS79aRJbABP1rhBBBQt_2K0130_assertion wasGeneratedBy ECO_0000203 NP357579.RAxx8lWiTKNZppE3wKfm89TS79aRJbABP1rhBBBQt_2K0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP357579.RAxx8lWiTKNZppE3wKfm89TS79aRJbABP1rhBBBQt_2K0130_provenance.