Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP776467.RANThyA9Di7tQVgswQJi_qA0XX43OSVxP8QX4Vs-I1okA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP776467.RANThyA9Di7tQVgswQJi_qA0XX43OSVxP8QX4Vs-I1okA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP776467.RANThyA9Di7tQVgswQJi_qA0XX43OSVxP8QX4Vs-I1okA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP776467.RANThyA9Di7tQVgswQJi_qA0XX43OSVxP8QX4Vs-I1okA130_provenance.
- NP776467.RANThyA9Di7tQVgswQJi_qA0XX43OSVxP8QX4Vs-I1okA130_assertion description "[Here, we describe a unique patient with a small isolated 9p terminal deletion, characterized by array-CGH and FISH, who shows a complex phenotype with multiple physical anomalies, resembling the 9p-syndrome, disorder of sex development with gonadoblastoma, congenital heart defect and epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776467.RANThyA9Di7tQVgswQJi_qA0XX43OSVxP8QX4Vs-I1okA130_provenance.
- NP776467.RANThyA9Di7tQVgswQJi_qA0XX43OSVxP8QX4Vs-I1okA130_assertion evidence source_evidence_literature NP776467.RANThyA9Di7tQVgswQJi_qA0XX43OSVxP8QX4Vs-I1okA130_provenance.
- NP776467.RANThyA9Di7tQVgswQJi_qA0XX43OSVxP8QX4Vs-I1okA130_assertion SIO_000772 22821627 NP776467.RANThyA9Di7tQVgswQJi_qA0XX43OSVxP8QX4Vs-I1okA130_provenance.
- NP776467.RANThyA9Di7tQVgswQJi_qA0XX43OSVxP8QX4Vs-I1okA130_assertion wasDerivedFrom befree-20140225 NP776467.RANThyA9Di7tQVgswQJi_qA0XX43OSVxP8QX4Vs-I1okA130_provenance.
- NP776467.RANThyA9Di7tQVgswQJi_qA0XX43OSVxP8QX4Vs-I1okA130_assertion wasGeneratedBy ECO_0000203 NP776467.RANThyA9Di7tQVgswQJi_qA0XX43OSVxP8QX4Vs-I1okA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP776467.RANThyA9Di7tQVgswQJi_qA0XX43OSVxP8QX4Vs-I1okA130_provenance.