Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP567849.RA1XLIcA6GdZSAMustjdYWsdOtKsMlRnk3zvY8F7CZECM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP567849.RA1XLIcA6GdZSAMustjdYWsdOtKsMlRnk3zvY8F7CZECM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP567849.RA1XLIcA6GdZSAMustjdYWsdOtKsMlRnk3zvY8F7CZECM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP567849.RA1XLIcA6GdZSAMustjdYWsdOtKsMlRnk3zvY8F7CZECM130_provenance.
- NP567849.RA1XLIcA6GdZSAMustjdYWsdOtKsMlRnk3zvY8F7CZECM130_assertion description "[The existence of the C4A-CYP21P-TNXA/TNXB locus might not be common in CAH patients with 21-hydroxylase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP567849.RA1XLIcA6GdZSAMustjdYWsdOtKsMlRnk3zvY8F7CZECM130_provenance.
- NP567849.RA1XLIcA6GdZSAMustjdYWsdOtKsMlRnk3zvY8F7CZECM130_assertion evidence source_evidence_literature NP567849.RA1XLIcA6GdZSAMustjdYWsdOtKsMlRnk3zvY8F7CZECM130_provenance.
- NP567849.RA1XLIcA6GdZSAMustjdYWsdOtKsMlRnk3zvY8F7CZECM130_assertion SIO_000772 15684714 NP567849.RA1XLIcA6GdZSAMustjdYWsdOtKsMlRnk3zvY8F7CZECM130_provenance.
- NP567849.RA1XLIcA6GdZSAMustjdYWsdOtKsMlRnk3zvY8F7CZECM130_assertion wasDerivedFrom befree-20140225 NP567849.RA1XLIcA6GdZSAMustjdYWsdOtKsMlRnk3zvY8F7CZECM130_provenance.
- NP567849.RA1XLIcA6GdZSAMustjdYWsdOtKsMlRnk3zvY8F7CZECM130_assertion wasGeneratedBy ECO_0000203 NP567849.RA1XLIcA6GdZSAMustjdYWsdOtKsMlRnk3zvY8F7CZECM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP567849.RA1XLIcA6GdZSAMustjdYWsdOtKsMlRnk3zvY8F7CZECM130_provenance.