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- source_evidence_literature type ECO_0000212 NP1313553.RALbdu0L4-VB6pSfuInw1gOSxcs3eE7fMfLZ0vTe2cZY8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1313553.RALbdu0L4-VB6pSfuInw1gOSxcs3eE7fMfLZ0vTe2cZY8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1313553.RALbdu0L4-VB6pSfuInw1gOSxcs3eE7fMfLZ0vTe2cZY8130_provenance.
- NP1313553.RALbdu0L4-VB6pSfuInw1gOSxcs3eE7fMfLZ0vTe2cZY8130_assertion description "[In summary, missense mutations within the exons of the androgen receptor gene encoding the steroid-binding domain of the receptor are common causes of both partial and complete forms of androgen insensitivity syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1313553.RALbdu0L4-VB6pSfuInw1gOSxcs3eE7fMfLZ0vTe2cZY8130_provenance.
- NP1313553.RALbdu0L4-VB6pSfuInw1gOSxcs3eE7fMfLZ0vTe2cZY8130_assertion evidence source_evidence_literature NP1313553.RALbdu0L4-VB6pSfuInw1gOSxcs3eE7fMfLZ0vTe2cZY8130_provenance.
- NP1313553.RALbdu0L4-VB6pSfuInw1gOSxcs3eE7fMfLZ0vTe2cZY8130_assertion SIO_000772 7581399 NP1313553.RALbdu0L4-VB6pSfuInw1gOSxcs3eE7fMfLZ0vTe2cZY8130_provenance.
- NP1313553.RALbdu0L4-VB6pSfuInw1gOSxcs3eE7fMfLZ0vTe2cZY8130_assertion wasDerivedFrom befree-2016 NP1313553.RALbdu0L4-VB6pSfuInw1gOSxcs3eE7fMfLZ0vTe2cZY8130_provenance.
- NP1313553.RALbdu0L4-VB6pSfuInw1gOSxcs3eE7fMfLZ0vTe2cZY8130_assertion wasGeneratedBy ECO_0000203 NP1313553.RALbdu0L4-VB6pSfuInw1gOSxcs3eE7fMfLZ0vTe2cZY8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1313553.RALbdu0L4-VB6pSfuInw1gOSxcs3eE7fMfLZ0vTe2cZY8130_provenance.