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- source_evidence_literature type ECO_0000212 NP1380668.RATH33nL4ahxlsdYcZq-irC_yTu4n3NaHYrCQXS-_G3Ys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1380668.RATH33nL4ahxlsdYcZq-irC_yTu4n3NaHYrCQXS-_G3Ys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1380668.RATH33nL4ahxlsdYcZq-irC_yTu4n3NaHYrCQXS-_G3Ys130_provenance.
- NP1380668.RATH33nL4ahxlsdYcZq-irC_yTu4n3NaHYrCQXS-_G3Ys130_assertion description "[Androgen receptor point mutations as the underlying molecular defect in 2 patients with androgen insensitivity syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1380668.RATH33nL4ahxlsdYcZq-irC_yTu4n3NaHYrCQXS-_G3Ys130_provenance.
- NP1380668.RATH33nL4ahxlsdYcZq-irC_yTu4n3NaHYrCQXS-_G3Ys130_assertion evidence source_evidence_literature NP1380668.RATH33nL4ahxlsdYcZq-irC_yTu4n3NaHYrCQXS-_G3Ys130_provenance.
- NP1380668.RATH33nL4ahxlsdYcZq-irC_yTu4n3NaHYrCQXS-_G3Ys130_assertion SIO_000772 9302173 NP1380668.RATH33nL4ahxlsdYcZq-irC_yTu4n3NaHYrCQXS-_G3Ys130_provenance.
- NP1380668.RATH33nL4ahxlsdYcZq-irC_yTu4n3NaHYrCQXS-_G3Ys130_assertion wasDerivedFrom befree-2016 NP1380668.RATH33nL4ahxlsdYcZq-irC_yTu4n3NaHYrCQXS-_G3Ys130_provenance.
- NP1380668.RATH33nL4ahxlsdYcZq-irC_yTu4n3NaHYrCQXS-_G3Ys130_assertion wasGeneratedBy ECO_0000203 NP1380668.RATH33nL4ahxlsdYcZq-irC_yTu4n3NaHYrCQXS-_G3Ys130_provenance.
- befree-2016 importedOn "2016-02-19" NP1380668.RATH33nL4ahxlsdYcZq-irC_yTu4n3NaHYrCQXS-_G3Ys130_provenance.