Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP383054.RAi15dWl9YOZZb6to75kKsQuD13Yf9XoWeenyqD5fh-GM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP383054.RAi15dWl9YOZZb6to75kKsQuD13Yf9XoWeenyqD5fh-GM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP383054.RAi15dWl9YOZZb6to75kKsQuD13Yf9XoWeenyqD5fh-GM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP383054.RAi15dWl9YOZZb6to75kKsQuD13Yf9XoWeenyqD5fh-GM130_provenance.
- befree-2016 importedOn "2016-02-19" NP383054.RAi15dWl9YOZZb6to75kKsQuD13Yf9XoWeenyqD5fh-GM130_provenance.
- NP383054.RAi15dWl9YOZZb6to75kKsQuD13Yf9XoWeenyqD5fh-GM130_assertion wasGeneratedBy ECO_0000203 NP383054.RAi15dWl9YOZZb6to75kKsQuD13Yf9XoWeenyqD5fh-GM130_provenance.
- NP383054.RAi15dWl9YOZZb6to75kKsQuD13Yf9XoWeenyqD5fh-GM130_assertion wasDerivedFrom befree-2016 NP383054.RAi15dWl9YOZZb6to75kKsQuD13Yf9XoWeenyqD5fh-GM130_provenance.
- NP383054.RAi15dWl9YOZZb6to75kKsQuD13Yf9XoWeenyqD5fh-GM130_assertion SIO_000772 12573815 NP383054.RAi15dWl9YOZZb6to75kKsQuD13Yf9XoWeenyqD5fh-GM130_provenance.
- NP383054.RAi15dWl9YOZZb6to75kKsQuD13Yf9XoWeenyqD5fh-GM130_assertion evidence source_evidence_literature NP383054.RAi15dWl9YOZZb6to75kKsQuD13Yf9XoWeenyqD5fh-GM130_provenance.
- NP383054.RAi15dWl9YOZZb6to75kKsQuD13Yf9XoWeenyqD5fh-GM130_assertion description "[Defects that interrupt the AR open-reading frame have been traced to a number of distinct types of genetic alterations, have been identified in widely separated segments of the AR gene, and are invariably associated with the phenotype of complete androgen insensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP383054.RAi15dWl9YOZZb6to75kKsQuD13Yf9XoWeenyqD5fh-GM130_provenance.