Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP286429.RAlu2aLvqxCMiPBIL2drOqDcWz5CNnfkktl1eCDk7f0As130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP286429.RAlu2aLvqxCMiPBIL2drOqDcWz5CNnfkktl1eCDk7f0As130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP286429.RAlu2aLvqxCMiPBIL2drOqDcWz5CNnfkktl1eCDk7f0As130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP286429.RAlu2aLvqxCMiPBIL2drOqDcWz5CNnfkktl1eCDk7f0As130_provenance.
- NP286429.RAlu2aLvqxCMiPBIL2drOqDcWz5CNnfkktl1eCDk7f0As130_assertion description "[SF1 mutations causing adrenal failure in humans are rare and are more likely to be associated with significant underandrogenization and gonadal dysfunction in 46,XY individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP286429.RAlu2aLvqxCMiPBIL2drOqDcWz5CNnfkktl1eCDk7f0As130_provenance.
- NP286429.RAlu2aLvqxCMiPBIL2drOqDcWz5CNnfkktl1eCDk7f0As130_assertion evidence source_evidence_literature NP286429.RAlu2aLvqxCMiPBIL2drOqDcWz5CNnfkktl1eCDk7f0As130_provenance.
- NP286429.RAlu2aLvqxCMiPBIL2drOqDcWz5CNnfkktl1eCDk7f0As130_assertion SIO_000772 16684822 NP286429.RAlu2aLvqxCMiPBIL2drOqDcWz5CNnfkktl1eCDk7f0As130_provenance.
- NP286429.RAlu2aLvqxCMiPBIL2drOqDcWz5CNnfkktl1eCDk7f0As130_assertion wasDerivedFrom befree-20140225 NP286429.RAlu2aLvqxCMiPBIL2drOqDcWz5CNnfkktl1eCDk7f0As130_provenance.
- NP286429.RAlu2aLvqxCMiPBIL2drOqDcWz5CNnfkktl1eCDk7f0As130_assertion wasGeneratedBy ECO_0000203 NP286429.RAlu2aLvqxCMiPBIL2drOqDcWz5CNnfkktl1eCDk7f0As130_provenance.
- befree-20140225 importedOn "2014-02-25" NP286429.RAlu2aLvqxCMiPBIL2drOqDcWz5CNnfkktl1eCDk7f0As130_provenance.