Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_provenance.
- NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_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." NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_provenance.
- NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_assertion evidence source_evidence_literature NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_provenance.
- NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_assertion SIO_000772 15639189 NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_provenance.
- NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_assertion wasDerivedFrom befree-20150227 NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_provenance.
- NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_assertion wasGeneratedBy ECO_0000203 NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_provenance.