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- source_evidence_literature type ECO_0000212 NP762654.RAnYPjy401O0q33PesEuXcP-ofS-b68hoBfgTxb3uOeBc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP762654.RAnYPjy401O0q33PesEuXcP-ofS-b68hoBfgTxb3uOeBc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP762654.RAnYPjy401O0q33PesEuXcP-ofS-b68hoBfgTxb3uOeBc130_provenance.
- NP762654.RAnYPjy401O0q33PesEuXcP-ofS-b68hoBfgTxb3uOeBc130_assertion description "[The authors report detailed clinical and developmental assessment of 3 brothers who were found to carry a novel mutation in the ARX gene associated with a relatively mild phenotype of static global developmental delay and early hand preference.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762654.RAnYPjy401O0q33PesEuXcP-ofS-b68hoBfgTxb3uOeBc130_provenance.
- NP762654.RAnYPjy401O0q33PesEuXcP-ofS-b68hoBfgTxb3uOeBc130_assertion evidence source_evidence_literature NP762654.RAnYPjy401O0q33PesEuXcP-ofS-b68hoBfgTxb3uOeBc130_provenance.
- NP762654.RAnYPjy401O0q33PesEuXcP-ofS-b68hoBfgTxb3uOeBc130_assertion SIO_000772 22922607 NP762654.RAnYPjy401O0q33PesEuXcP-ofS-b68hoBfgTxb3uOeBc130_provenance.
- NP762654.RAnYPjy401O0q33PesEuXcP-ofS-b68hoBfgTxb3uOeBc130_assertion wasDerivedFrom befree-20140225 NP762654.RAnYPjy401O0q33PesEuXcP-ofS-b68hoBfgTxb3uOeBc130_provenance.
- NP762654.RAnYPjy401O0q33PesEuXcP-ofS-b68hoBfgTxb3uOeBc130_assertion wasGeneratedBy ECO_0000203 NP762654.RAnYPjy401O0q33PesEuXcP-ofS-b68hoBfgTxb3uOeBc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP762654.RAnYPjy401O0q33PesEuXcP-ofS-b68hoBfgTxb3uOeBc130_provenance.