Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP316621.RAyjX4hC-ZVqjG4pcbk3QtBql_sgRhpm3Vr-F0b2HHTuc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP316621.RAyjX4hC-ZVqjG4pcbk3QtBql_sgRhpm3Vr-F0b2HHTuc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316621.RAyjX4hC-ZVqjG4pcbk3QtBql_sgRhpm3Vr-F0b2HHTuc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316621.RAyjX4hC-ZVqjG4pcbk3QtBql_sgRhpm3Vr-F0b2HHTuc130_provenance.
- NP316621.RAyjX4hC-ZVqjG4pcbk3QtBql_sgRhpm3Vr-F0b2HHTuc130_assertion description "[In this paper we report detailed autopsy data of a malformed male newborn with 5p trisomy due to a de novo inverted 5p duplication, inv dup (5)(p13.1----p15.3), and we compare these data with the findings in previous reports on 5p trisomy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316621.RAyjX4hC-ZVqjG4pcbk3QtBql_sgRhpm3Vr-F0b2HHTuc130_provenance.
- NP316621.RAyjX4hC-ZVqjG4pcbk3QtBql_sgRhpm3Vr-F0b2HHTuc130_assertion evidence source_evidence_literature NP316621.RAyjX4hC-ZVqjG4pcbk3QtBql_sgRhpm3Vr-F0b2HHTuc130_provenance.
- NP316621.RAyjX4hC-ZVqjG4pcbk3QtBql_sgRhpm3Vr-F0b2HHTuc130_assertion SIO_000772 3621654 NP316621.RAyjX4hC-ZVqjG4pcbk3QtBql_sgRhpm3Vr-F0b2HHTuc130_provenance.
- NP316621.RAyjX4hC-ZVqjG4pcbk3QtBql_sgRhpm3Vr-F0b2HHTuc130_assertion wasDerivedFrom befree-20140225 NP316621.RAyjX4hC-ZVqjG4pcbk3QtBql_sgRhpm3Vr-F0b2HHTuc130_provenance.
- NP316621.RAyjX4hC-ZVqjG4pcbk3QtBql_sgRhpm3Vr-F0b2HHTuc130_assertion wasGeneratedBy ECO_0000203 NP316621.RAyjX4hC-ZVqjG4pcbk3QtBql_sgRhpm3Vr-F0b2HHTuc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP316621.RAyjX4hC-ZVqjG4pcbk3QtBql_sgRhpm3Vr-F0b2HHTuc130_provenance.