Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP831224.RAZXFgjTDB05s5QeQ-s6CMO7DkWd5dpkZwsSPYCxLhOPI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP831224.RAZXFgjTDB05s5QeQ-s6CMO7DkWd5dpkZwsSPYCxLhOPI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP831224.RAZXFgjTDB05s5QeQ-s6CMO7DkWd5dpkZwsSPYCxLhOPI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP831224.RAZXFgjTDB05s5QeQ-s6CMO7DkWd5dpkZwsSPYCxLhOPI130_provenance.
- NP831224.RAZXFgjTDB05s5QeQ-s6CMO7DkWd5dpkZwsSPYCxLhOPI130_assertion description "[Altered expression of several mental retardation genes such as UBE3A (Angelman Syndrome), ZEB2 (Mowat-Wilson Syndrome) and MEF2C was also found in TCF4-depleted cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831224.RAZXFgjTDB05s5QeQ-s6CMO7DkWd5dpkZwsSPYCxLhOPI130_provenance.
- NP831224.RAZXFgjTDB05s5QeQ-s6CMO7DkWd5dpkZwsSPYCxLhOPI130_assertion evidence source_evidence_literature NP831224.RAZXFgjTDB05s5QeQ-s6CMO7DkWd5dpkZwsSPYCxLhOPI130_provenance.
- NP831224.RAZXFgjTDB05s5QeQ-s6CMO7DkWd5dpkZwsSPYCxLhOPI130_assertion SIO_000772 24058414 NP831224.RAZXFgjTDB05s5QeQ-s6CMO7DkWd5dpkZwsSPYCxLhOPI130_provenance.
- NP831224.RAZXFgjTDB05s5QeQ-s6CMO7DkWd5dpkZwsSPYCxLhOPI130_assertion wasDerivedFrom befree-20150227 NP831224.RAZXFgjTDB05s5QeQ-s6CMO7DkWd5dpkZwsSPYCxLhOPI130_provenance.
- NP831224.RAZXFgjTDB05s5QeQ-s6CMO7DkWd5dpkZwsSPYCxLhOPI130_assertion wasGeneratedBy ECO_0000203 NP831224.RAZXFgjTDB05s5QeQ-s6CMO7DkWd5dpkZwsSPYCxLhOPI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP831224.RAZXFgjTDB05s5QeQ-s6CMO7DkWd5dpkZwsSPYCxLhOPI130_provenance.