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- source_evidence_literature type ECO_0000212 NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_provenance.
- NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_assertion description "[These results indicate that the SRJ domain is dispensable for these functions of CITED2 in mice and that mutations clustering in the SRJ region are unlikely to be the sole cause of the malformations observed in patients with sporadic CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_provenance.
- NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_assertion evidence source_evidence_literature NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_provenance.
- NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_assertion SIO_000772 23082118 NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_provenance.
- NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_assertion wasDerivedFrom befree-20150227 NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_provenance.
- NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_assertion wasGeneratedBy ECO_0000203 NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_provenance.