Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP665560.RA1q0Ql7CelzUI113M_ipYGrJQNltOg2MhnA4NLuTSxmA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP665560.RA1q0Ql7CelzUI113M_ipYGrJQNltOg2MhnA4NLuTSxmA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP665560.RA1q0Ql7CelzUI113M_ipYGrJQNltOg2MhnA4NLuTSxmA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP665560.RA1q0Ql7CelzUI113M_ipYGrJQNltOg2MhnA4NLuTSxmA130_provenance.
- NP665560.RA1q0Ql7CelzUI113M_ipYGrJQNltOg2MhnA4NLuTSxmA130_assertion description "[We report the cytogenetic and molecular characterization of a 22.3-Mb pure interstitial duplication of chromosome 7q, dup(7)(q31.2-->q33) in a 4-year-old girl with growth restriction, short stature, speech delay, inguinal hernia, strabismus and intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665560.RA1q0Ql7CelzUI113M_ipYGrJQNltOg2MhnA4NLuTSxmA130_provenance.
- NP665560.RA1q0Ql7CelzUI113M_ipYGrJQNltOg2MhnA4NLuTSxmA130_assertion evidence source_evidence_literature NP665560.RA1q0Ql7CelzUI113M_ipYGrJQNltOg2MhnA4NLuTSxmA130_provenance.
- NP665560.RA1q0Ql7CelzUI113M_ipYGrJQNltOg2MhnA4NLuTSxmA130_assertion SIO_000772 22303804 NP665560.RA1q0Ql7CelzUI113M_ipYGrJQNltOg2MhnA4NLuTSxmA130_provenance.
- NP665560.RA1q0Ql7CelzUI113M_ipYGrJQNltOg2MhnA4NLuTSxmA130_assertion wasDerivedFrom befree-20140225 NP665560.RA1q0Ql7CelzUI113M_ipYGrJQNltOg2MhnA4NLuTSxmA130_provenance.
- NP665560.RA1q0Ql7CelzUI113M_ipYGrJQNltOg2MhnA4NLuTSxmA130_assertion wasGeneratedBy ECO_0000203 NP665560.RA1q0Ql7CelzUI113M_ipYGrJQNltOg2MhnA4NLuTSxmA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP665560.RA1q0Ql7CelzUI113M_ipYGrJQNltOg2MhnA4NLuTSxmA130_provenance.