Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP441806.RAH5P3LqPMs38ZpKaemzSiWHIY2Nwp3eYxQkI5Q0jXYag130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP441806.RAH5P3LqPMs38ZpKaemzSiWHIY2Nwp3eYxQkI5Q0jXYag130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP441806.RAH5P3LqPMs38ZpKaemzSiWHIY2Nwp3eYxQkI5Q0jXYag130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP441806.RAH5P3LqPMs38ZpKaemzSiWHIY2Nwp3eYxQkI5Q0jXYag130_provenance.
- befree-20150227 importedOn "2015-02-27" NP441806.RAH5P3LqPMs38ZpKaemzSiWHIY2Nwp3eYxQkI5Q0jXYag130_provenance.
- NP441806.RAH5P3LqPMs38ZpKaemzSiWHIY2Nwp3eYxQkI5Q0jXYag130_assertion wasGeneratedBy ECO_0000203 NP441806.RAH5P3LqPMs38ZpKaemzSiWHIY2Nwp3eYxQkI5Q0jXYag130_provenance.
- NP441806.RAH5P3LqPMs38ZpKaemzSiWHIY2Nwp3eYxQkI5Q0jXYag130_assertion wasDerivedFrom befree-20150227 NP441806.RAH5P3LqPMs38ZpKaemzSiWHIY2Nwp3eYxQkI5Q0jXYag130_provenance.
- NP441806.RAH5P3LqPMs38ZpKaemzSiWHIY2Nwp3eYxQkI5Q0jXYag130_assertion SIO_000772 19568270 NP441806.RAH5P3LqPMs38ZpKaemzSiWHIY2Nwp3eYxQkI5Q0jXYag130_provenance.
- NP441806.RAH5P3LqPMs38ZpKaemzSiWHIY2Nwp3eYxQkI5Q0jXYag130_assertion evidence source_evidence_literature NP441806.RAH5P3LqPMs38ZpKaemzSiWHIY2Nwp3eYxQkI5Q0jXYag130_provenance.
- NP441806.RAH5P3LqPMs38ZpKaemzSiWHIY2Nwp3eYxQkI5Q0jXYag130_assertion description "[Our results are consistent with the hypothesis that hemizygosity of the GTF2IRD1 and GTF2I genes might be involved in the facial dysmorphisms and in the specific motor and cognitive deficits observed in WBS patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441806.RAH5P3LqPMs38ZpKaemzSiWHIY2Nwp3eYxQkI5Q0jXYag130_provenance.