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- source_evidence_literature type ECO_0000212 NP470453.RATBJylAZzwEwdLsBN_g26is1tjiKfrlpeRZhsmdlDwf4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470453.RATBJylAZzwEwdLsBN_g26is1tjiKfrlpeRZhsmdlDwf4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470453.RATBJylAZzwEwdLsBN_g26is1tjiKfrlpeRZhsmdlDwf4130_provenance.
- NP470453.RATBJylAZzwEwdLsBN_g26is1tjiKfrlpeRZhsmdlDwf4130_assertion description "[Suspected microdeletion syndromes such as deletion 22q11.2, Williams-Beuren and Angelman syndromes were excluded before array-CGH analysis was performed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470453.RATBJylAZzwEwdLsBN_g26is1tjiKfrlpeRZhsmdlDwf4130_provenance.
- NP470453.RATBJylAZzwEwdLsBN_g26is1tjiKfrlpeRZhsmdlDwf4130_assertion evidence source_evidence_literature NP470453.RATBJylAZzwEwdLsBN_g26is1tjiKfrlpeRZhsmdlDwf4130_provenance.
- NP470453.RATBJylAZzwEwdLsBN_g26is1tjiKfrlpeRZhsmdlDwf4130_assertion SIO_000772 17901693 NP470453.RATBJylAZzwEwdLsBN_g26is1tjiKfrlpeRZhsmdlDwf4130_provenance.
- NP470453.RATBJylAZzwEwdLsBN_g26is1tjiKfrlpeRZhsmdlDwf4130_assertion wasDerivedFrom befree-20150227 NP470453.RATBJylAZzwEwdLsBN_g26is1tjiKfrlpeRZhsmdlDwf4130_provenance.
- NP470453.RATBJylAZzwEwdLsBN_g26is1tjiKfrlpeRZhsmdlDwf4130_assertion wasGeneratedBy ECO_0000203 NP470453.RATBJylAZzwEwdLsBN_g26is1tjiKfrlpeRZhsmdlDwf4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP470453.RATBJylAZzwEwdLsBN_g26is1tjiKfrlpeRZhsmdlDwf4130_provenance.