Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP413589.RAQ7SdvnJ3RDmhs0rSKjtjRsCEi1HqDSUugdFk54Ln6Ak130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP413589.RAQ7SdvnJ3RDmhs0rSKjtjRsCEi1HqDSUugdFk54Ln6Ak130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP413589.RAQ7SdvnJ3RDmhs0rSKjtjRsCEi1HqDSUugdFk54Ln6Ak130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP413589.RAQ7SdvnJ3RDmhs0rSKjtjRsCEi1HqDSUugdFk54Ln6Ak130_provenance.
- NP413589.RAQ7SdvnJ3RDmhs0rSKjtjRsCEi1HqDSUugdFk54Ln6Ak130_assertion description "[More recently, heterozygous NR5A1 mutations have been identified in a substantial proportion of patients with 46,XY disorders of sex development (46,XY DSD) without adrenal insufficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP413589.RAQ7SdvnJ3RDmhs0rSKjtjRsCEi1HqDSUugdFk54Ln6Ak130_provenance.
- NP413589.RAQ7SdvnJ3RDmhs0rSKjtjRsCEi1HqDSUugdFk54Ln6Ak130_assertion evidence source_evidence_literature NP413589.RAQ7SdvnJ3RDmhs0rSKjtjRsCEi1HqDSUugdFk54Ln6Ak130_provenance.
- NP413589.RAQ7SdvnJ3RDmhs0rSKjtjRsCEi1HqDSUugdFk54Ln6Ak130_assertion SIO_000772 20595937 NP413589.RAQ7SdvnJ3RDmhs0rSKjtjRsCEi1HqDSUugdFk54Ln6Ak130_provenance.
- NP413589.RAQ7SdvnJ3RDmhs0rSKjtjRsCEi1HqDSUugdFk54Ln6Ak130_assertion wasDerivedFrom befree-20150227 NP413589.RAQ7SdvnJ3RDmhs0rSKjtjRsCEi1HqDSUugdFk54Ln6Ak130_provenance.
- NP413589.RAQ7SdvnJ3RDmhs0rSKjtjRsCEi1HqDSUugdFk54Ln6Ak130_assertion wasGeneratedBy ECO_0000203 NP413589.RAQ7SdvnJ3RDmhs0rSKjtjRsCEi1HqDSUugdFk54Ln6Ak130_provenance.
- befree-20150227 importedOn "2015-02-27" NP413589.RAQ7SdvnJ3RDmhs0rSKjtjRsCEi1HqDSUugdFk54Ln6Ak130_provenance.