Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1127466.RAHj9E6S0YIm0Ay8AEYm9ONlAJpE_Oew2S7mMROR1TShg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1127466.RAHj9E6S0YIm0Ay8AEYm9ONlAJpE_Oew2S7mMROR1TShg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1127466.RAHj9E6S0YIm0Ay8AEYm9ONlAJpE_Oew2S7mMROR1TShg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1127466.RAHj9E6S0YIm0Ay8AEYm9ONlAJpE_Oew2S7mMROR1TShg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1127466.RAHj9E6S0YIm0Ay8AEYm9ONlAJpE_Oew2S7mMROR1TShg130_provenance.
- NP1127466.RAHj9E6S0YIm0Ay8AEYm9ONlAJpE_Oew2S7mMROR1TShg130_assertion wasGeneratedBy ECO_0000203 NP1127466.RAHj9E6S0YIm0Ay8AEYm9ONlAJpE_Oew2S7mMROR1TShg130_provenance.
- NP1127466.RAHj9E6S0YIm0Ay8AEYm9ONlAJpE_Oew2S7mMROR1TShg130_assertion wasDerivedFrom befree-2016 NP1127466.RAHj9E6S0YIm0Ay8AEYm9ONlAJpE_Oew2S7mMROR1TShg130_provenance.
- NP1127466.RAHj9E6S0YIm0Ay8AEYm9ONlAJpE_Oew2S7mMROR1TShg130_assertion SIO_000772 24222239 NP1127466.RAHj9E6S0YIm0Ay8AEYm9ONlAJpE_Oew2S7mMROR1TShg130_provenance.
- NP1127466.RAHj9E6S0YIm0Ay8AEYm9ONlAJpE_Oew2S7mMROR1TShg130_assertion evidence source_evidence_literature NP1127466.RAHj9E6S0YIm0Ay8AEYm9ONlAJpE_Oew2S7mMROR1TShg130_provenance.
- NP1127466.RAHj9E6S0YIm0Ay8AEYm9ONlAJpE_Oew2S7mMROR1TShg130_assertion description "[To determine the incidence of GATA1 mutations in a cohort of DS patients and the applicability of these mutations as a clonal marker to detect minimal residual disease, we screened 198 samples of 169 patients with DS for mutations in GATA1 exon 2 by direct sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1127466.RAHj9E6S0YIm0Ay8AEYm9ONlAJpE_Oew2S7mMROR1TShg130_provenance.