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- source_evidence_literature type ECO_0000212 NP496388.RA-NVYExAGTIvXCHsufN7Dx6IPwL-xjmUtKsRpmSr1KqA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP496388.RA-NVYExAGTIvXCHsufN7Dx6IPwL-xjmUtKsRpmSr1KqA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP496388.RA-NVYExAGTIvXCHsufN7Dx6IPwL-xjmUtKsRpmSr1KqA130_provenance.
- NP496388.RA-NVYExAGTIvXCHsufN7Dx6IPwL-xjmUtKsRpmSr1KqA130_assertion description "[Prenatal exclusion of Crouzon syndrome by mutation analysis of FGFR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496388.RA-NVYExAGTIvXCHsufN7Dx6IPwL-xjmUtKsRpmSr1KqA130_provenance.
- NP496388.RA-NVYExAGTIvXCHsufN7Dx6IPwL-xjmUtKsRpmSr1KqA130_assertion evidence source_evidence_literature NP496388.RA-NVYExAGTIvXCHsufN7Dx6IPwL-xjmUtKsRpmSr1KqA130_provenance.
- NP496388.RA-NVYExAGTIvXCHsufN7Dx6IPwL-xjmUtKsRpmSr1KqA130_assertion SIO_000772 15916101 NP496388.RA-NVYExAGTIvXCHsufN7Dx6IPwL-xjmUtKsRpmSr1KqA130_provenance.
- NP496388.RA-NVYExAGTIvXCHsufN7Dx6IPwL-xjmUtKsRpmSr1KqA130_assertion wasDerivedFrom befree-2016 NP496388.RA-NVYExAGTIvXCHsufN7Dx6IPwL-xjmUtKsRpmSr1KqA130_provenance.
- NP496388.RA-NVYExAGTIvXCHsufN7Dx6IPwL-xjmUtKsRpmSr1KqA130_assertion wasGeneratedBy ECO_0000203 NP496388.RA-NVYExAGTIvXCHsufN7Dx6IPwL-xjmUtKsRpmSr1KqA130_provenance.
- befree-2016 importedOn "2016-02-19" NP496388.RA-NVYExAGTIvXCHsufN7Dx6IPwL-xjmUtKsRpmSr1KqA130_provenance.