Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1005251.RAdo4eotUa9DhwYzx1SXSOCUp7WzSe3SL_J9LDv6JqyW0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1005251.RAdo4eotUa9DhwYzx1SXSOCUp7WzSe3SL_J9LDv6JqyW0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1005251.RAdo4eotUa9DhwYzx1SXSOCUp7WzSe3SL_J9LDv6JqyW0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1005251.RAdo4eotUa9DhwYzx1SXSOCUp7WzSe3SL_J9LDv6JqyW0130_provenance.
- NP1005251.RAdo4eotUa9DhwYzx1SXSOCUp7WzSe3SL_J9LDv6JqyW0130_assertion description "[The TBX1 gene is considered to be the major candidate gene for the main features in 22q11.2 deletion syndrome, including congenital heart malformations, (para)thyroid hypoplasia, and craniofacial abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1005251.RAdo4eotUa9DhwYzx1SXSOCUp7WzSe3SL_J9LDv6JqyW0130_provenance.
- NP1005251.RAdo4eotUa9DhwYzx1SXSOCUp7WzSe3SL_J9LDv6JqyW0130_assertion evidence source_evidence_literature NP1005251.RAdo4eotUa9DhwYzx1SXSOCUp7WzSe3SL_J9LDv6JqyW0130_provenance.
- NP1005251.RAdo4eotUa9DhwYzx1SXSOCUp7WzSe3SL_J9LDv6JqyW0130_assertion SIO_000772 22893440 NP1005251.RAdo4eotUa9DhwYzx1SXSOCUp7WzSe3SL_J9LDv6JqyW0130_provenance.
- NP1005251.RAdo4eotUa9DhwYzx1SXSOCUp7WzSe3SL_J9LDv6JqyW0130_assertion wasDerivedFrom befree-2016 NP1005251.RAdo4eotUa9DhwYzx1SXSOCUp7WzSe3SL_J9LDv6JqyW0130_provenance.
- NP1005251.RAdo4eotUa9DhwYzx1SXSOCUp7WzSe3SL_J9LDv6JqyW0130_assertion wasGeneratedBy ECO_0000203 NP1005251.RAdo4eotUa9DhwYzx1SXSOCUp7WzSe3SL_J9LDv6JqyW0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1005251.RAdo4eotUa9DhwYzx1SXSOCUp7WzSe3SL_J9LDv6JqyW0130_provenance.