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- source_evidence_literature type ECO_0000212 NP490466.RAHeDBZ_z0RzbVk6OyngvPx2kOp_RjXCnVYlVvIP7Ldnk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP490466.RAHeDBZ_z0RzbVk6OyngvPx2kOp_RjXCnVYlVvIP7Ldnk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP490466.RAHeDBZ_z0RzbVk6OyngvPx2kOp_RjXCnVYlVvIP7Ldnk130_provenance.
- NP490466.RAHeDBZ_z0RzbVk6OyngvPx2kOp_RjXCnVYlVvIP7Ldnk130_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." NP490466.RAHeDBZ_z0RzbVk6OyngvPx2kOp_RjXCnVYlVvIP7Ldnk130_provenance.
- NP490466.RAHeDBZ_z0RzbVk6OyngvPx2kOp_RjXCnVYlVvIP7Ldnk130_assertion evidence source_evidence_literature NP490466.RAHeDBZ_z0RzbVk6OyngvPx2kOp_RjXCnVYlVvIP7Ldnk130_provenance.
- NP490466.RAHeDBZ_z0RzbVk6OyngvPx2kOp_RjXCnVYlVvIP7Ldnk130_assertion SIO_000772 19568270 NP490466.RAHeDBZ_z0RzbVk6OyngvPx2kOp_RjXCnVYlVvIP7Ldnk130_provenance.
- NP490466.RAHeDBZ_z0RzbVk6OyngvPx2kOp_RjXCnVYlVvIP7Ldnk130_assertion wasDerivedFrom befree-20140225 NP490466.RAHeDBZ_z0RzbVk6OyngvPx2kOp_RjXCnVYlVvIP7Ldnk130_provenance.
- NP490466.RAHeDBZ_z0RzbVk6OyngvPx2kOp_RjXCnVYlVvIP7Ldnk130_assertion wasGeneratedBy ECO_0000203 NP490466.RAHeDBZ_z0RzbVk6OyngvPx2kOp_RjXCnVYlVvIP7Ldnk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP490466.RAHeDBZ_z0RzbVk6OyngvPx2kOp_RjXCnVYlVvIP7Ldnk130_provenance.