Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP903619.RAVuj91I2VVZz2r-nul1hFdO-bA0GDPA0jF78qky90OYQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP903619.RAVuj91I2VVZz2r-nul1hFdO-bA0GDPA0jF78qky90OYQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP903619.RAVuj91I2VVZz2r-nul1hFdO-bA0GDPA0jF78qky90OYQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP903619.RAVuj91I2VVZz2r-nul1hFdO-bA0GDPA0jF78qky90OYQ130_provenance.
- NP903619.RAVuj91I2VVZz2r-nul1hFdO-bA0GDPA0jF78qky90OYQ130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP903619.RAVuj91I2VVZz2r-nul1hFdO-bA0GDPA0jF78qky90OYQ130_provenance.
- NP903619.RAVuj91I2VVZz2r-nul1hFdO-bA0GDPA0jF78qky90OYQ130_assertion evidence source_evidence_literature NP903619.RAVuj91I2VVZz2r-nul1hFdO-bA0GDPA0jF78qky90OYQ130_provenance.
- NP903619.RAVuj91I2VVZz2r-nul1hFdO-bA0GDPA0jF78qky90OYQ130_assertion SIO_000772 15639189 NP903619.RAVuj91I2VVZz2r-nul1hFdO-bA0GDPA0jF78qky90OYQ130_provenance.
- NP903619.RAVuj91I2VVZz2r-nul1hFdO-bA0GDPA0jF78qky90OYQ130_assertion wasDerivedFrom befree-20140225 NP903619.RAVuj91I2VVZz2r-nul1hFdO-bA0GDPA0jF78qky90OYQ130_provenance.
- NP903619.RAVuj91I2VVZz2r-nul1hFdO-bA0GDPA0jF78qky90OYQ130_assertion wasGeneratedBy ECO_0000203 NP903619.RAVuj91I2VVZz2r-nul1hFdO-bA0GDPA0jF78qky90OYQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP903619.RAVuj91I2VVZz2r-nul1hFdO-bA0GDPA0jF78qky90OYQ130_provenance.