Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP531774.RAzB4OrMoUlH_p0ob4eOH8V415RNcNx92NHUpjkuZ5_k4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP531774.RAzB4OrMoUlH_p0ob4eOH8V415RNcNx92NHUpjkuZ5_k4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP531774.RAzB4OrMoUlH_p0ob4eOH8V415RNcNx92NHUpjkuZ5_k4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP531774.RAzB4OrMoUlH_p0ob4eOH8V415RNcNx92NHUpjkuZ5_k4130_provenance.
- NP531774.RAzB4OrMoUlH_p0ob4eOH8V415RNcNx92NHUpjkuZ5_k4130_assertion description "[X-linked adrenoleukodystrophy (X-ALD) is a severe neurodegenerative disease caused by loss of function of the peroxisomal transporter ABCD1 (ALD), which results in accumulation of very long chain fatty acids (VLCFAs) in organs and serum, central demyelination and peripheral axonopathy and Addison's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531774.RAzB4OrMoUlH_p0ob4eOH8V415RNcNx92NHUpjkuZ5_k4130_provenance.
- NP531774.RAzB4OrMoUlH_p0ob4eOH8V415RNcNx92NHUpjkuZ5_k4130_assertion evidence source_evidence_literature NP531774.RAzB4OrMoUlH_p0ob4eOH8V415RNcNx92NHUpjkuZ5_k4130_provenance.
- NP531774.RAzB4OrMoUlH_p0ob4eOH8V415RNcNx92NHUpjkuZ5_k4130_assertion SIO_000772 15489218 NP531774.RAzB4OrMoUlH_p0ob4eOH8V415RNcNx92NHUpjkuZ5_k4130_provenance.
- NP531774.RAzB4OrMoUlH_p0ob4eOH8V415RNcNx92NHUpjkuZ5_k4130_assertion wasDerivedFrom befree-20140225 NP531774.RAzB4OrMoUlH_p0ob4eOH8V415RNcNx92NHUpjkuZ5_k4130_provenance.
- NP531774.RAzB4OrMoUlH_p0ob4eOH8V415RNcNx92NHUpjkuZ5_k4130_assertion wasGeneratedBy ECO_0000203 NP531774.RAzB4OrMoUlH_p0ob4eOH8V415RNcNx92NHUpjkuZ5_k4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP531774.RAzB4OrMoUlH_p0ob4eOH8V415RNcNx92NHUpjkuZ5_k4130_provenance.