Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP430696.RAB6RyXuwhTT86EZU25WDMJQHxcHvT2ZtqRNj8Q99YFz4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP430696.RAB6RyXuwhTT86EZU25WDMJQHxcHvT2ZtqRNj8Q99YFz4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP430696.RAB6RyXuwhTT86EZU25WDMJQHxcHvT2ZtqRNj8Q99YFz4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP430696.RAB6RyXuwhTT86EZU25WDMJQHxcHvT2ZtqRNj8Q99YFz4130_provenance.
- NP430696.RAB6RyXuwhTT86EZU25WDMJQHxcHvT2ZtqRNj8Q99YFz4130_assertion wasGeneratedBy ECO_0000203 NP430696.RAB6RyXuwhTT86EZU25WDMJQHxcHvT2ZtqRNj8Q99YFz4130_provenance.
- NP430696.RAB6RyXuwhTT86EZU25WDMJQHxcHvT2ZtqRNj8Q99YFz4130_assertion wasDerivedFrom befree-20140225 NP430696.RAB6RyXuwhTT86EZU25WDMJQHxcHvT2ZtqRNj8Q99YFz4130_provenance.
- NP430696.RAB6RyXuwhTT86EZU25WDMJQHxcHvT2ZtqRNj8Q99YFz4130_assertion SIO_000772 18055909 NP430696.RAB6RyXuwhTT86EZU25WDMJQHxcHvT2ZtqRNj8Q99YFz4130_provenance.
- NP430696.RAB6RyXuwhTT86EZU25WDMJQHxcHvT2ZtqRNj8Q99YFz4130_assertion evidence source_evidence_literature NP430696.RAB6RyXuwhTT86EZU25WDMJQHxcHvT2ZtqRNj8Q99YFz4130_provenance.
- NP430696.RAB6RyXuwhTT86EZU25WDMJQHxcHvT2ZtqRNj8Q99YFz4130_assertion description "[These data suggest that non-synonymous GATA4 sequence variants are found in a small percentage of patients with septal defects and are very uncommonly found in patients with conotruncal defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430696.RAB6RyXuwhTT86EZU25WDMJQHxcHvT2ZtqRNj8Q99YFz4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP430696.RAB6RyXuwhTT86EZU25WDMJQHxcHvT2ZtqRNj8Q99YFz4130_provenance.