Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP478815.RAD9kp_vNo41KyMEvlokkbdiiIP3HdzgbaX6d-WCs4F4Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478815.RAD9kp_vNo41KyMEvlokkbdiiIP3HdzgbaX6d-WCs4F4Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478815.RAD9kp_vNo41KyMEvlokkbdiiIP3HdzgbaX6d-WCs4F4Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478815.RAD9kp_vNo41KyMEvlokkbdiiIP3HdzgbaX6d-WCs4F4Q130_provenance.
- NP478815.RAD9kp_vNo41KyMEvlokkbdiiIP3HdzgbaX6d-WCs4F4Q130_assertion description "[The existence of the C4A-CYP21P-TNXA/TNXB locus might not be common in CAH patients with 21-hydroxylase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478815.RAD9kp_vNo41KyMEvlokkbdiiIP3HdzgbaX6d-WCs4F4Q130_provenance.
- NP478815.RAD9kp_vNo41KyMEvlokkbdiiIP3HdzgbaX6d-WCs4F4Q130_assertion evidence source_evidence_literature NP478815.RAD9kp_vNo41KyMEvlokkbdiiIP3HdzgbaX6d-WCs4F4Q130_provenance.
- NP478815.RAD9kp_vNo41KyMEvlokkbdiiIP3HdzgbaX6d-WCs4F4Q130_assertion SIO_000772 15684714 NP478815.RAD9kp_vNo41KyMEvlokkbdiiIP3HdzgbaX6d-WCs4F4Q130_provenance.
- NP478815.RAD9kp_vNo41KyMEvlokkbdiiIP3HdzgbaX6d-WCs4F4Q130_assertion wasDerivedFrom befree-2016 NP478815.RAD9kp_vNo41KyMEvlokkbdiiIP3HdzgbaX6d-WCs4F4Q130_provenance.
- NP478815.RAD9kp_vNo41KyMEvlokkbdiiIP3HdzgbaX6d-WCs4F4Q130_assertion wasGeneratedBy ECO_0000203 NP478815.RAD9kp_vNo41KyMEvlokkbdiiIP3HdzgbaX6d-WCs4F4Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP478815.RAD9kp_vNo41KyMEvlokkbdiiIP3HdzgbaX6d-WCs4F4Q130_provenance.