Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP425448.RAmA73_dlmZ0ntrtNbclO10SzhELbDtX3kuJpsZlM3jeE130_assertion> ?p ?o ?g. }
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- NP425448.RAmA73_dlmZ0ntrtNbclO10SzhELbDtX3kuJpsZlM3jeE130_assertion type Assertion NP425448.RAmA73_dlmZ0ntrtNbclO10SzhELbDtX3kuJpsZlM3jeE130_head.
- NP425448.RAmA73_dlmZ0ntrtNbclO10SzhELbDtX3kuJpsZlM3jeE130_assertion description "[Recessive GJA1 mutations cause Hallermann-Streiff syndrome, a disorder showing substantial overlap with ODDD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP425448.RAmA73_dlmZ0ntrtNbclO10SzhELbDtX3kuJpsZlM3jeE130_provenance.
- NP425448.RAmA73_dlmZ0ntrtNbclO10SzhELbDtX3kuJpsZlM3jeE130_assertion evidence source_evidence_literature NP425448.RAmA73_dlmZ0ntrtNbclO10SzhELbDtX3kuJpsZlM3jeE130_provenance.
- NP425448.RAmA73_dlmZ0ntrtNbclO10SzhELbDtX3kuJpsZlM3jeE130_assertion SIO_000772 21871435 NP425448.RAmA73_dlmZ0ntrtNbclO10SzhELbDtX3kuJpsZlM3jeE130_provenance.
- NP425448.RAmA73_dlmZ0ntrtNbclO10SzhELbDtX3kuJpsZlM3jeE130_assertion wasDerivedFrom befree-20150227 NP425448.RAmA73_dlmZ0ntrtNbclO10SzhELbDtX3kuJpsZlM3jeE130_provenance.
- NP425448.RAmA73_dlmZ0ntrtNbclO10SzhELbDtX3kuJpsZlM3jeE130_assertion wasGeneratedBy ECO_0000203 NP425448.RAmA73_dlmZ0ntrtNbclO10SzhELbDtX3kuJpsZlM3jeE130_provenance.