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- NP699303.RAEN5cDXOIs-1716RkwtiNT3ZTxBeJVSzLWxP3Rdp0LhI130_assertion type Assertion NP699303.RAEN5cDXOIs-1716RkwtiNT3ZTxBeJVSzLWxP3Rdp0LhI130_head.
- NP699303.RAEN5cDXOIs-1716RkwtiNT3ZTxBeJVSzLWxP3Rdp0LhI130_assertion wasGeneratedBy ECO_0000203 NP699303.RAEN5cDXOIs-1716RkwtiNT3ZTxBeJVSzLWxP3Rdp0LhI130_provenance.
- NP699303.RAEN5cDXOIs-1716RkwtiNT3ZTxBeJVSzLWxP3Rdp0LhI130_assertion wasDerivedFrom befree-2016 NP699303.RAEN5cDXOIs-1716RkwtiNT3ZTxBeJVSzLWxP3Rdp0LhI130_provenance.
- NP699303.RAEN5cDXOIs-1716RkwtiNT3ZTxBeJVSzLWxP3Rdp0LhI130_assertion SIO_000772 18941922 NP699303.RAEN5cDXOIs-1716RkwtiNT3ZTxBeJVSzLWxP3Rdp0LhI130_provenance.
- NP699303.RAEN5cDXOIs-1716RkwtiNT3ZTxBeJVSzLWxP3Rdp0LhI130_assertion evidence source_evidence_literature NP699303.RAEN5cDXOIs-1716RkwtiNT3ZTxBeJVSzLWxP3Rdp0LhI130_provenance.
- NP699303.RAEN5cDXOIs-1716RkwtiNT3ZTxBeJVSzLWxP3Rdp0LhI130_assertion description "[These are the first data showing a significant association of non-GLA-derived sequence variants with the cardiac phenotype in Fabry disease that may in part explain the great phenotypic variability of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699303.RAEN5cDXOIs-1716RkwtiNT3ZTxBeJVSzLWxP3Rdp0LhI130_provenance.