Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP234036.RANZoZ_K0AXOx2zYOVhOTRUStcnHUfWuVwAMZ1Qvt2tsI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP234036.RANZoZ_K0AXOx2zYOVhOTRUStcnHUfWuVwAMZ1Qvt2tsI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP234036.RANZoZ_K0AXOx2zYOVhOTRUStcnHUfWuVwAMZ1Qvt2tsI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP234036.RANZoZ_K0AXOx2zYOVhOTRUStcnHUfWuVwAMZ1Qvt2tsI130_provenance.
- NP234036.RANZoZ_K0AXOx2zYOVhOTRUStcnHUfWuVwAMZ1Qvt2tsI130_assertion description "[X-linked adrenoleukodystrophy (X-ALD) is an inherited disease with clinical heterogeneity varying from presymptomatic individuals to rapidly progressive cerebral ALD forms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP234036.RANZoZ_K0AXOx2zYOVhOTRUStcnHUfWuVwAMZ1Qvt2tsI130_provenance.
- NP234036.RANZoZ_K0AXOx2zYOVhOTRUStcnHUfWuVwAMZ1Qvt2tsI130_assertion evidence source_evidence_literature NP234036.RANZoZ_K0AXOx2zYOVhOTRUStcnHUfWuVwAMZ1Qvt2tsI130_provenance.
- NP234036.RANZoZ_K0AXOx2zYOVhOTRUStcnHUfWuVwAMZ1Qvt2tsI130_assertion SIO_000772 21340162 NP234036.RANZoZ_K0AXOx2zYOVhOTRUStcnHUfWuVwAMZ1Qvt2tsI130_provenance.
- NP234036.RANZoZ_K0AXOx2zYOVhOTRUStcnHUfWuVwAMZ1Qvt2tsI130_assertion wasDerivedFrom befree-20150227 NP234036.RANZoZ_K0AXOx2zYOVhOTRUStcnHUfWuVwAMZ1Qvt2tsI130_provenance.
- NP234036.RANZoZ_K0AXOx2zYOVhOTRUStcnHUfWuVwAMZ1Qvt2tsI130_assertion wasGeneratedBy ECO_0000203 NP234036.RANZoZ_K0AXOx2zYOVhOTRUStcnHUfWuVwAMZ1Qvt2tsI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP234036.RANZoZ_K0AXOx2zYOVhOTRUStcnHUfWuVwAMZ1Qvt2tsI130_provenance.