Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP780004.RAqK3RhcdcbOJFg2BXvxQnbw7_cF6M__cjTwEENCumjxs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP780004.RAqK3RhcdcbOJFg2BXvxQnbw7_cF6M__cjTwEENCumjxs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP780004.RAqK3RhcdcbOJFg2BXvxQnbw7_cF6M__cjTwEENCumjxs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP780004.RAqK3RhcdcbOJFg2BXvxQnbw7_cF6M__cjTwEENCumjxs130_provenance.
- NP780004.RAqK3RhcdcbOJFg2BXvxQnbw7_cF6M__cjTwEENCumjxs130_assertion description "[The patient with hypergonadotropic hypogonadism was diagnosed with BPES due to a new FOXL2 gene mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP780004.RAqK3RhcdcbOJFg2BXvxQnbw7_cF6M__cjTwEENCumjxs130_provenance.
- NP780004.RAqK3RhcdcbOJFg2BXvxQnbw7_cF6M__cjTwEENCumjxs130_assertion evidence source_evidence_literature NP780004.RAqK3RhcdcbOJFg2BXvxQnbw7_cF6M__cjTwEENCumjxs130_provenance.
- NP780004.RAqK3RhcdcbOJFg2BXvxQnbw7_cF6M__cjTwEENCumjxs130_assertion SIO_000772 19969293 NP780004.RAqK3RhcdcbOJFg2BXvxQnbw7_cF6M__cjTwEENCumjxs130_provenance.
- NP780004.RAqK3RhcdcbOJFg2BXvxQnbw7_cF6M__cjTwEENCumjxs130_assertion wasDerivedFrom befree-2016 NP780004.RAqK3RhcdcbOJFg2BXvxQnbw7_cF6M__cjTwEENCumjxs130_provenance.
- NP780004.RAqK3RhcdcbOJFg2BXvxQnbw7_cF6M__cjTwEENCumjxs130_assertion wasGeneratedBy ECO_0000203 NP780004.RAqK3RhcdcbOJFg2BXvxQnbw7_cF6M__cjTwEENCumjxs130_provenance.
- befree-2016 importedOn "2016-02-19" NP780004.RAqK3RhcdcbOJFg2BXvxQnbw7_cF6M__cjTwEENCumjxs130_provenance.