Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP133199.RA4XQZ4JsB3DJZzk8HAcp57GCQBGV30PL8_WJ8vskn8Bw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP133199.RA4XQZ4JsB3DJZzk8HAcp57GCQBGV30PL8_WJ8vskn8Bw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP133199.RA4XQZ4JsB3DJZzk8HAcp57GCQBGV30PL8_WJ8vskn8Bw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP133199.RA4XQZ4JsB3DJZzk8HAcp57GCQBGV30PL8_WJ8vskn8Bw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP133199.RA4XQZ4JsB3DJZzk8HAcp57GCQBGV30PL8_WJ8vskn8Bw130_provenance.
- NP133199.RA4XQZ4JsB3DJZzk8HAcp57GCQBGV30PL8_WJ8vskn8Bw130_assertion wasGeneratedBy ECO_0000203 NP133199.RA4XQZ4JsB3DJZzk8HAcp57GCQBGV30PL8_WJ8vskn8Bw130_provenance.
- NP133199.RA4XQZ4JsB3DJZzk8HAcp57GCQBGV30PL8_WJ8vskn8Bw130_assertion wasDerivedFrom gad-20150221 NP133199.RA4XQZ4JsB3DJZzk8HAcp57GCQBGV30PL8_WJ8vskn8Bw130_provenance.
- NP133199.RA4XQZ4JsB3DJZzk8HAcp57GCQBGV30PL8_WJ8vskn8Bw130_assertion SIO_000772 20541041 NP133199.RA4XQZ4JsB3DJZzk8HAcp57GCQBGV30PL8_WJ8vskn8Bw130_provenance.
- NP133199.RA4XQZ4JsB3DJZzk8HAcp57GCQBGV30PL8_WJ8vskn8Bw130_assertion evidence source_evidence_literature NP133199.RA4XQZ4JsB3DJZzk8HAcp57GCQBGV30PL8_WJ8vskn8Bw130_provenance.
- NP133199.RA4XQZ4JsB3DJZzk8HAcp57GCQBGV30PL8_WJ8vskn8Bw130_assertion description "[Compound mutation carriers are associated with a more severe phenotype than single mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133199.RA4XQZ4JsB3DJZzk8HAcp57GCQBGV30PL8_WJ8vskn8Bw130_provenance.