Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP526300.RAUrpQw4fG653TO7MuwpUnC2KOmEfSFtpBx2nNWdsRJU4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP526300.RAUrpQw4fG653TO7MuwpUnC2KOmEfSFtpBx2nNWdsRJU4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP526300.RAUrpQw4fG653TO7MuwpUnC2KOmEfSFtpBx2nNWdsRJU4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP526300.RAUrpQw4fG653TO7MuwpUnC2KOmEfSFtpBx2nNWdsRJU4130_provenance.
- NP526300.RAUrpQw4fG653TO7MuwpUnC2KOmEfSFtpBx2nNWdsRJU4130_assertion description "[However, the frequency distribution of KLK1 promoter among VUR patients with or without CRI (A, 50.0% and 67.5%; B, 17.9% and 8.3%; H, 14.3% and 18.3%; K, 17.9% and 5.8%, respectively) was statistically different (P = 0.008).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP526300.RAUrpQw4fG653TO7MuwpUnC2KOmEfSFtpBx2nNWdsRJU4130_provenance.
- NP526300.RAUrpQw4fG653TO7MuwpUnC2KOmEfSFtpBx2nNWdsRJU4130_assertion evidence source_evidence_literature NP526300.RAUrpQw4fG653TO7MuwpUnC2KOmEfSFtpBx2nNWdsRJU4130_provenance.
- NP526300.RAUrpQw4fG653TO7MuwpUnC2KOmEfSFtpBx2nNWdsRJU4130_assertion SIO_000772 15086490 NP526300.RAUrpQw4fG653TO7MuwpUnC2KOmEfSFtpBx2nNWdsRJU4130_provenance.
- NP526300.RAUrpQw4fG653TO7MuwpUnC2KOmEfSFtpBx2nNWdsRJU4130_assertion wasDerivedFrom befree-20150227 NP526300.RAUrpQw4fG653TO7MuwpUnC2KOmEfSFtpBx2nNWdsRJU4130_provenance.
- NP526300.RAUrpQw4fG653TO7MuwpUnC2KOmEfSFtpBx2nNWdsRJU4130_assertion wasGeneratedBy ECO_0000203 NP526300.RAUrpQw4fG653TO7MuwpUnC2KOmEfSFtpBx2nNWdsRJU4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP526300.RAUrpQw4fG653TO7MuwpUnC2KOmEfSFtpBx2nNWdsRJU4130_provenance.