Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP867059.RAlWad6ec2Oc2BENgaQFfZVkt11-2bTTRaUqFyRyJFbf4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP867059.RAlWad6ec2Oc2BENgaQFfZVkt11-2bTTRaUqFyRyJFbf4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867059.RAlWad6ec2Oc2BENgaQFfZVkt11-2bTTRaUqFyRyJFbf4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867059.RAlWad6ec2Oc2BENgaQFfZVkt11-2bTTRaUqFyRyJFbf4130_provenance.
- NP867059.RAlWad6ec2Oc2BENgaQFfZVkt11-2bTTRaUqFyRyJFbf4130_assertion wasGeneratedBy ECO_0000203 NP867059.RAlWad6ec2Oc2BENgaQFfZVkt11-2bTTRaUqFyRyJFbf4130_provenance.
- NP867059.RAlWad6ec2Oc2BENgaQFfZVkt11-2bTTRaUqFyRyJFbf4130_assertion wasDerivedFrom befree-20140225 NP867059.RAlWad6ec2Oc2BENgaQFfZVkt11-2bTTRaUqFyRyJFbf4130_provenance.
- NP867059.RAlWad6ec2Oc2BENgaQFfZVkt11-2bTTRaUqFyRyJFbf4130_assertion SIO_000772 10521100 NP867059.RAlWad6ec2Oc2BENgaQFfZVkt11-2bTTRaUqFyRyJFbf4130_provenance.
- NP867059.RAlWad6ec2Oc2BENgaQFfZVkt11-2bTTRaUqFyRyJFbf4130_assertion evidence source_evidence_literature NP867059.RAlWad6ec2Oc2BENgaQFfZVkt11-2bTTRaUqFyRyJFbf4130_provenance.
- NP867059.RAlWad6ec2Oc2BENgaQFfZVkt11-2bTTRaUqFyRyJFbf4130_assertion description "[Four patients (three with idiopathic hirsutism, one with ovarian hyperandrogenism) and one control were carriers of CYP21 mutations typically associated with classic congenital adrenal hyperplasia but had normal basal and ACTH-stimulated 17-hydroxyprogesterone levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867059.RAlWad6ec2Oc2BENgaQFfZVkt11-2bTTRaUqFyRyJFbf4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP867059.RAlWad6ec2Oc2BENgaQFfZVkt11-2bTTRaUqFyRyJFbf4130_provenance.