Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP584544.RAYRz2QpQmr32eWVd3d3vrGq0w4oL1sXXG8sn_nUnpEqs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP584544.RAYRz2QpQmr32eWVd3d3vrGq0w4oL1sXXG8sn_nUnpEqs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584544.RAYRz2QpQmr32eWVd3d3vrGq0w4oL1sXXG8sn_nUnpEqs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584544.RAYRz2QpQmr32eWVd3d3vrGq0w4oL1sXXG8sn_nUnpEqs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP584544.RAYRz2QpQmr32eWVd3d3vrGq0w4oL1sXXG8sn_nUnpEqs130_provenance.
- NP584544.RAYRz2QpQmr32eWVd3d3vrGq0w4oL1sXXG8sn_nUnpEqs130_assertion wasGeneratedBy ECO_0000203 NP584544.RAYRz2QpQmr32eWVd3d3vrGq0w4oL1sXXG8sn_nUnpEqs130_provenance.
- NP584544.RAYRz2QpQmr32eWVd3d3vrGq0w4oL1sXXG8sn_nUnpEqs130_assertion wasDerivedFrom befree-20150227 NP584544.RAYRz2QpQmr32eWVd3d3vrGq0w4oL1sXXG8sn_nUnpEqs130_provenance.
- NP584544.RAYRz2QpQmr32eWVd3d3vrGq0w4oL1sXXG8sn_nUnpEqs130_assertion SIO_000772 14685826 NP584544.RAYRz2QpQmr32eWVd3d3vrGq0w4oL1sXXG8sn_nUnpEqs130_provenance.
- NP584544.RAYRz2QpQmr32eWVd3d3vrGq0w4oL1sXXG8sn_nUnpEqs130_assertion evidence source_evidence_literature NP584544.RAYRz2QpQmr32eWVd3d3vrGq0w4oL1sXXG8sn_nUnpEqs130_provenance.
- NP584544.RAYRz2QpQmr32eWVd3d3vrGq0w4oL1sXXG8sn_nUnpEqs130_assertion description "[Alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency (Schindler/Kanzaki disease) is a clinically and pathologically heterogeneous genetic disease with a wide spectrum including an early onset neuroaxonal dystrophy (Schindler disease) and late onset angiokeratoma corporis diffusum (Kanzaki disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584544.RAYRz2QpQmr32eWVd3d3vrGq0w4oL1sXXG8sn_nUnpEqs130_provenance.