Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP500437.RAhKZJYldI4xpOBAczaKEOESN-0pENC9rMffPCA2-t9uo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP500437.RAhKZJYldI4xpOBAczaKEOESN-0pENC9rMffPCA2-t9uo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP500437.RAhKZJYldI4xpOBAczaKEOESN-0pENC9rMffPCA2-t9uo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP500437.RAhKZJYldI4xpOBAczaKEOESN-0pENC9rMffPCA2-t9uo130_provenance.
- NP500437.RAhKZJYldI4xpOBAczaKEOESN-0pENC9rMffPCA2-t9uo130_assertion description "[Six out of 28 (21%) patients with Sertoli cell-only syndrome, and two out of 18 (11%) patients with maturation arrest had mutations in the USP26 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500437.RAhKZJYldI4xpOBAczaKEOESN-0pENC9rMffPCA2-t9uo130_provenance.
- NP500437.RAhKZJYldI4xpOBAczaKEOESN-0pENC9rMffPCA2-t9uo130_assertion evidence source_evidence_literature NP500437.RAhKZJYldI4xpOBAczaKEOESN-0pENC9rMffPCA2-t9uo130_provenance.
- NP500437.RAhKZJYldI4xpOBAczaKEOESN-0pENC9rMffPCA2-t9uo130_assertion SIO_000772 15970005 NP500437.RAhKZJYldI4xpOBAczaKEOESN-0pENC9rMffPCA2-t9uo130_provenance.
- NP500437.RAhKZJYldI4xpOBAczaKEOESN-0pENC9rMffPCA2-t9uo130_assertion wasDerivedFrom befree-2016 NP500437.RAhKZJYldI4xpOBAczaKEOESN-0pENC9rMffPCA2-t9uo130_provenance.
- NP500437.RAhKZJYldI4xpOBAczaKEOESN-0pENC9rMffPCA2-t9uo130_assertion wasGeneratedBy ECO_0000203 NP500437.RAhKZJYldI4xpOBAczaKEOESN-0pENC9rMffPCA2-t9uo130_provenance.
- befree-2016 importedOn "2016-02-19" NP500437.RAhKZJYldI4xpOBAczaKEOESN-0pENC9rMffPCA2-t9uo130_provenance.