Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_provenance.
- NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_assertion description "[Mutations of the androgen receptor gene causing androgen insensitivity syndrome in 46, XY individuals, result in phenotypes ranging from complete female to ambiguous genitalia to males with minor degrees of undervirilization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_provenance.
- NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_assertion evidence source_evidence_literature NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_provenance.
- NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_assertion SIO_000772 10502786 NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_provenance.
- NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_assertion wasDerivedFrom befree-2016 NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_provenance.
- NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_assertion wasGeneratedBy ECO_0000203 NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_provenance.
- befree-2016 importedOn "2016-02-19" NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_provenance.