Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP699315.RAWmiK7XEKYAhh0fnBgyS7BNvGdHwGqHPiQnObUCc3saw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP699315.RAWmiK7XEKYAhh0fnBgyS7BNvGdHwGqHPiQnObUCc3saw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP699315.RAWmiK7XEKYAhh0fnBgyS7BNvGdHwGqHPiQnObUCc3saw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP699315.RAWmiK7XEKYAhh0fnBgyS7BNvGdHwGqHPiQnObUCc3saw130_provenance.
- NP699315.RAWmiK7XEKYAhh0fnBgyS7BNvGdHwGqHPiQnObUCc3saw130_assertion description "[The�infant had a ventricular septal defect, hand and skull anomalies, and hyperglycaemia compatible with haploinsufficiency of TBX20, GLI3, and GCK genes, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699315.RAWmiK7XEKYAhh0fnBgyS7BNvGdHwGqHPiQnObUCc3saw130_provenance.
- NP699315.RAWmiK7XEKYAhh0fnBgyS7BNvGdHwGqHPiQnObUCc3saw130_assertion evidence source_evidence_literature NP699315.RAWmiK7XEKYAhh0fnBgyS7BNvGdHwGqHPiQnObUCc3saw130_provenance.
- NP699315.RAWmiK7XEKYAhh0fnBgyS7BNvGdHwGqHPiQnObUCc3saw130_assertion SIO_000772 20933618 NP699315.RAWmiK7XEKYAhh0fnBgyS7BNvGdHwGqHPiQnObUCc3saw130_provenance.
- NP699315.RAWmiK7XEKYAhh0fnBgyS7BNvGdHwGqHPiQnObUCc3saw130_assertion wasDerivedFrom befree-20140225 NP699315.RAWmiK7XEKYAhh0fnBgyS7BNvGdHwGqHPiQnObUCc3saw130_provenance.
- NP699315.RAWmiK7XEKYAhh0fnBgyS7BNvGdHwGqHPiQnObUCc3saw130_assertion wasGeneratedBy ECO_0000203 NP699315.RAWmiK7XEKYAhh0fnBgyS7BNvGdHwGqHPiQnObUCc3saw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP699315.RAWmiK7XEKYAhh0fnBgyS7BNvGdHwGqHPiQnObUCc3saw130_provenance.