Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP279566.RAsGYjtrh2l4XlYSYP9pCkwyFHVRkAUUfrVF_ksIaOmfE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP279566.RAsGYjtrh2l4XlYSYP9pCkwyFHVRkAUUfrVF_ksIaOmfE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP279566.RAsGYjtrh2l4XlYSYP9pCkwyFHVRkAUUfrVF_ksIaOmfE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP279566.RAsGYjtrh2l4XlYSYP9pCkwyFHVRkAUUfrVF_ksIaOmfE130_provenance.
- NP279566.RAsGYjtrh2l4XlYSYP9pCkwyFHVRkAUUfrVF_ksIaOmfE130_assertion description "[X-linked spinal and bulbar muscular atrophy (SBMA), a motor neuron disease associated with androgen insensitivity, is caused by androgen receptor gene mutations with an increased number of tandem CAG repeats in exon 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279566.RAsGYjtrh2l4XlYSYP9pCkwyFHVRkAUUfrVF_ksIaOmfE130_provenance.
- NP279566.RAsGYjtrh2l4XlYSYP9pCkwyFHVRkAUUfrVF_ksIaOmfE130_assertion evidence source_evidence_literature NP279566.RAsGYjtrh2l4XlYSYP9pCkwyFHVRkAUUfrVF_ksIaOmfE130_provenance.
- NP279566.RAsGYjtrh2l4XlYSYP9pCkwyFHVRkAUUfrVF_ksIaOmfE130_assertion SIO_000772 1461383 NP279566.RAsGYjtrh2l4XlYSYP9pCkwyFHVRkAUUfrVF_ksIaOmfE130_provenance.
- NP279566.RAsGYjtrh2l4XlYSYP9pCkwyFHVRkAUUfrVF_ksIaOmfE130_assertion wasDerivedFrom befree-20140225 NP279566.RAsGYjtrh2l4XlYSYP9pCkwyFHVRkAUUfrVF_ksIaOmfE130_provenance.
- NP279566.RAsGYjtrh2l4XlYSYP9pCkwyFHVRkAUUfrVF_ksIaOmfE130_assertion wasGeneratedBy ECO_0000203 NP279566.RAsGYjtrh2l4XlYSYP9pCkwyFHVRkAUUfrVF_ksIaOmfE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP279566.RAsGYjtrh2l4XlYSYP9pCkwyFHVRkAUUfrVF_ksIaOmfE130_provenance.