Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP738997.RA-nFWzf3wCHKiA1UGy8kJx0hYg77k3OlUn13qU6TP26M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP738997.RA-nFWzf3wCHKiA1UGy8kJx0hYg77k3OlUn13qU6TP26M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP738997.RA-nFWzf3wCHKiA1UGy8kJx0hYg77k3OlUn13qU6TP26M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP738997.RA-nFWzf3wCHKiA1UGy8kJx0hYg77k3OlUn13qU6TP26M130_provenance.
- NP738997.RA-nFWzf3wCHKiA1UGy8kJx0hYg77k3OlUn13qU6TP26M130_assertion description "[arrayCGH analysis revealed a cryptic deletion of the region 4q24 in all eight patients selected with myeloid malignancies (3 MDS, 1 AML and 4 MPN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP738997.RA-nFWzf3wCHKiA1UGy8kJx0hYg77k3OlUn13qU6TP26M130_provenance.
- NP738997.RA-nFWzf3wCHKiA1UGy8kJx0hYg77k3OlUn13qU6TP26M130_assertion evidence source_evidence_literature NP738997.RA-nFWzf3wCHKiA1UGy8kJx0hYg77k3OlUn13qU6TP26M130_provenance.
- NP738997.RA-nFWzf3wCHKiA1UGy8kJx0hYg77k3OlUn13qU6TP26M130_assertion SIO_000772 23389918 NP738997.RA-nFWzf3wCHKiA1UGy8kJx0hYg77k3OlUn13qU6TP26M130_provenance.
- NP738997.RA-nFWzf3wCHKiA1UGy8kJx0hYg77k3OlUn13qU6TP26M130_assertion wasDerivedFrom befree-20140225 NP738997.RA-nFWzf3wCHKiA1UGy8kJx0hYg77k3OlUn13qU6TP26M130_provenance.
- NP738997.RA-nFWzf3wCHKiA1UGy8kJx0hYg77k3OlUn13qU6TP26M130_assertion wasGeneratedBy ECO_0000203 NP738997.RA-nFWzf3wCHKiA1UGy8kJx0hYg77k3OlUn13qU6TP26M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP738997.RA-nFWzf3wCHKiA1UGy8kJx0hYg77k3OlUn13qU6TP26M130_provenance.