Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP791225.RAMm06xBA7Ai-OPl0eBu-k7TBkIU5h1JF497ipfmg1HpU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP791225.RAMm06xBA7Ai-OPl0eBu-k7TBkIU5h1JF497ipfmg1HpU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP791225.RAMm06xBA7Ai-OPl0eBu-k7TBkIU5h1JF497ipfmg1HpU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP791225.RAMm06xBA7Ai-OPl0eBu-k7TBkIU5h1JF497ipfmg1HpU130_provenance.
- NP791225.RAMm06xBA7Ai-OPl0eBu-k7TBkIU5h1JF497ipfmg1HpU130_assertion description "[A similar issue of differential diagnosis was raised by a large 4.3 Mb 2q22.3q23.1 deletion encompassing ZEB2, the gene responsible for the Mowat-Wilson syndrome, whose signs may overlap with RSTS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791225.RAMm06xBA7Ai-OPl0eBu-k7TBkIU5h1JF497ipfmg1HpU130_provenance.
- NP791225.RAMm06xBA7Ai-OPl0eBu-k7TBkIU5h1JF497ipfmg1HpU130_assertion evidence source_evidence_literature NP791225.RAMm06xBA7Ai-OPl0eBu-k7TBkIU5h1JF497ipfmg1HpU130_provenance.
- NP791225.RAMm06xBA7Ai-OPl0eBu-k7TBkIU5h1JF497ipfmg1HpU130_assertion SIO_000772 20125191 NP791225.RAMm06xBA7Ai-OPl0eBu-k7TBkIU5h1JF497ipfmg1HpU130_provenance.
- NP791225.RAMm06xBA7Ai-OPl0eBu-k7TBkIU5h1JF497ipfmg1HpU130_assertion wasDerivedFrom befree-2016 NP791225.RAMm06xBA7Ai-OPl0eBu-k7TBkIU5h1JF497ipfmg1HpU130_provenance.
- NP791225.RAMm06xBA7Ai-OPl0eBu-k7TBkIU5h1JF497ipfmg1HpU130_assertion wasGeneratedBy ECO_0000203 NP791225.RAMm06xBA7Ai-OPl0eBu-k7TBkIU5h1JF497ipfmg1HpU130_provenance.
- befree-2016 importedOn "2016-02-19" NP791225.RAMm06xBA7Ai-OPl0eBu-k7TBkIU5h1JF497ipfmg1HpU130_provenance.