Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_provenance.
- NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_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." NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_provenance.
- NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_assertion evidence source_evidence_literature NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_provenance.
- NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_assertion SIO_000772 22893440 NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_provenance.
- NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_assertion wasDerivedFrom befree-20140225 NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_provenance.
- NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_assertion wasGeneratedBy ECO_0000203 NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_provenance.