Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP184644.RAMZ2dsB1AIp2dv9551NiggM-tlTHQ9E5149HhpFKrmCY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP184644.RAMZ2dsB1AIp2dv9551NiggM-tlTHQ9E5149HhpFKrmCY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP184644.RAMZ2dsB1AIp2dv9551NiggM-tlTHQ9E5149HhpFKrmCY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP184644.RAMZ2dsB1AIp2dv9551NiggM-tlTHQ9E5149HhpFKrmCY130_provenance.
- NP184644.RAMZ2dsB1AIp2dv9551NiggM-tlTHQ9E5149HhpFKrmCY130_assertion description "[Taken together, the results support the hypothesis that 12R-LOX, eLOX3, and perhaps an epoxide hydrolase function together in the normal process of skin differentiation, and that the loss of function mutations are the basis of the LOX-dependent form of NCIE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184644.RAMZ2dsB1AIp2dv9551NiggM-tlTHQ9E5149HhpFKrmCY130_provenance.
- NP184644.RAMZ2dsB1AIp2dv9551NiggM-tlTHQ9E5149HhpFKrmCY130_assertion evidence source_evidence_literature NP184644.RAMZ2dsB1AIp2dv9551NiggM-tlTHQ9E5149HhpFKrmCY130_provenance.
- NP184644.RAMZ2dsB1AIp2dv9551NiggM-tlTHQ9E5149HhpFKrmCY130_assertion SIO_000772 15629692 NP184644.RAMZ2dsB1AIp2dv9551NiggM-tlTHQ9E5149HhpFKrmCY130_provenance.
- NP184644.RAMZ2dsB1AIp2dv9551NiggM-tlTHQ9E5149HhpFKrmCY130_assertion wasDerivedFrom befree-20140225 NP184644.RAMZ2dsB1AIp2dv9551NiggM-tlTHQ9E5149HhpFKrmCY130_provenance.
- NP184644.RAMZ2dsB1AIp2dv9551NiggM-tlTHQ9E5149HhpFKrmCY130_assertion wasGeneratedBy ECO_0000203 NP184644.RAMZ2dsB1AIp2dv9551NiggM-tlTHQ9E5149HhpFKrmCY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP184644.RAMZ2dsB1AIp2dv9551NiggM-tlTHQ9E5149HhpFKrmCY130_provenance.