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- source_evidence_literature type ECO_0000212 NP425662.RAuj-LlB6rIdmQzm2AUTHhBig5DEARNi5f1yxdygqTgws130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP425662.RAuj-LlB6rIdmQzm2AUTHhBig5DEARNi5f1yxdygqTgws130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP425662.RAuj-LlB6rIdmQzm2AUTHhBig5DEARNi5f1yxdygqTgws130_provenance.
- NP425662.RAuj-LlB6rIdmQzm2AUTHhBig5DEARNi5f1yxdygqTgws130_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." NP425662.RAuj-LlB6rIdmQzm2AUTHhBig5DEARNi5f1yxdygqTgws130_provenance.
- NP425662.RAuj-LlB6rIdmQzm2AUTHhBig5DEARNi5f1yxdygqTgws130_assertion evidence source_evidence_literature NP425662.RAuj-LlB6rIdmQzm2AUTHhBig5DEARNi5f1yxdygqTgws130_provenance.
- NP425662.RAuj-LlB6rIdmQzm2AUTHhBig5DEARNi5f1yxdygqTgws130_assertion SIO_000772 21871435 NP425662.RAuj-LlB6rIdmQzm2AUTHhBig5DEARNi5f1yxdygqTgws130_provenance.
- NP425662.RAuj-LlB6rIdmQzm2AUTHhBig5DEARNi5f1yxdygqTgws130_assertion wasDerivedFrom befree-20150227 NP425662.RAuj-LlB6rIdmQzm2AUTHhBig5DEARNi5f1yxdygqTgws130_provenance.
- NP425662.RAuj-LlB6rIdmQzm2AUTHhBig5DEARNi5f1yxdygqTgws130_assertion wasGeneratedBy ECO_0000203 NP425662.RAuj-LlB6rIdmQzm2AUTHhBig5DEARNi5f1yxdygqTgws130_provenance.
- befree-20150227 importedOn "2015-02-27" NP425662.RAuj-LlB6rIdmQzm2AUTHhBig5DEARNi5f1yxdygqTgws130_provenance.