Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP813947.RAuEtcHcsM7-r44QtlIwnIWXTvAhjGLo7UCmCdQUXSasc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP813947.RAuEtcHcsM7-r44QtlIwnIWXTvAhjGLo7UCmCdQUXSasc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP813947.RAuEtcHcsM7-r44QtlIwnIWXTvAhjGLo7UCmCdQUXSasc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP813947.RAuEtcHcsM7-r44QtlIwnIWXTvAhjGLo7UCmCdQUXSasc130_provenance.
- NP813947.RAuEtcHcsM7-r44QtlIwnIWXTvAhjGLo7UCmCdQUXSasc130_assertion description "[A novel 8.5 MB dup(1)(p34.1p34.3) characterized by FISH in a child presenting with congenital heart defect and dysmorphic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP813947.RAuEtcHcsM7-r44QtlIwnIWXTvAhjGLo7UCmCdQUXSasc130_provenance.
- NP813947.RAuEtcHcsM7-r44QtlIwnIWXTvAhjGLo7UCmCdQUXSasc130_assertion evidence source_evidence_literature NP813947.RAuEtcHcsM7-r44QtlIwnIWXTvAhjGLo7UCmCdQUXSasc130_provenance.
- NP813947.RAuEtcHcsM7-r44QtlIwnIWXTvAhjGLo7UCmCdQUXSasc130_assertion SIO_000772 16892326 NP813947.RAuEtcHcsM7-r44QtlIwnIWXTvAhjGLo7UCmCdQUXSasc130_provenance.
- NP813947.RAuEtcHcsM7-r44QtlIwnIWXTvAhjGLo7UCmCdQUXSasc130_assertion wasDerivedFrom befree-20140225 NP813947.RAuEtcHcsM7-r44QtlIwnIWXTvAhjGLo7UCmCdQUXSasc130_provenance.
- NP813947.RAuEtcHcsM7-r44QtlIwnIWXTvAhjGLo7UCmCdQUXSasc130_assertion wasGeneratedBy ECO_0000203 NP813947.RAuEtcHcsM7-r44QtlIwnIWXTvAhjGLo7UCmCdQUXSasc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP813947.RAuEtcHcsM7-r44QtlIwnIWXTvAhjGLo7UCmCdQUXSasc130_provenance.