Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP425448.RAmA73_dlmZ0ntrtNbclO10SzhELbDtX3kuJpsZlM3jeE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP425448.RAmA73_dlmZ0ntrtNbclO10SzhELbDtX3kuJpsZlM3jeE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP425448.RAmA73_dlmZ0ntrtNbclO10SzhELbDtX3kuJpsZlM3jeE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP425448.RAmA73_dlmZ0ntrtNbclO10SzhELbDtX3kuJpsZlM3jeE130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP425448.RAmA73_dlmZ0ntrtNbclO10SzhELbDtX3kuJpsZlM3jeE130_provenance.