Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1322832.RAZMd8A-nV6oeo_DBhx9OICxXysnnGYNdtNuFqpJoB3wg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1322832.RAZMd8A-nV6oeo_DBhx9OICxXysnnGYNdtNuFqpJoB3wg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1322832.RAZMd8A-nV6oeo_DBhx9OICxXysnnGYNdtNuFqpJoB3wg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1322832.RAZMd8A-nV6oeo_DBhx9OICxXysnnGYNdtNuFqpJoB3wg130_provenance.
- NP1322832.RAZMd8A-nV6oeo_DBhx9OICxXysnnGYNdtNuFqpJoB3wg130_assertion description "[The absence of del(5q), trisomy 8 and 21, as well as the rarity of monosomy 7, contrasts with pooled published data and may reflect our exclusion of closely related disorders, in particular MDS with fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1322832.RAZMd8A-nV6oeo_DBhx9OICxXysnnGYNdtNuFqpJoB3wg130_provenance.
- NP1322832.RAZMd8A-nV6oeo_DBhx9OICxXysnnGYNdtNuFqpJoB3wg130_assertion evidence source_evidence_literature NP1322832.RAZMd8A-nV6oeo_DBhx9OICxXysnnGYNdtNuFqpJoB3wg130_provenance.
- NP1322832.RAZMd8A-nV6oeo_DBhx9OICxXysnnGYNdtNuFqpJoB3wg130_assertion SIO_000772 7819070 NP1322832.RAZMd8A-nV6oeo_DBhx9OICxXysnnGYNdtNuFqpJoB3wg130_provenance.
- NP1322832.RAZMd8A-nV6oeo_DBhx9OICxXysnnGYNdtNuFqpJoB3wg130_assertion wasDerivedFrom befree-2016 NP1322832.RAZMd8A-nV6oeo_DBhx9OICxXysnnGYNdtNuFqpJoB3wg130_provenance.
- NP1322832.RAZMd8A-nV6oeo_DBhx9OICxXysnnGYNdtNuFqpJoB3wg130_assertion wasGeneratedBy ECO_0000203 NP1322832.RAZMd8A-nV6oeo_DBhx9OICxXysnnGYNdtNuFqpJoB3wg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1322832.RAZMd8A-nV6oeo_DBhx9OICxXysnnGYNdtNuFqpJoB3wg130_provenance.