Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP581746.RA9wKc17bltftvooda1gkiIqfV1qmptwU4R_Vv2jFYo3g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP581746.RA9wKc17bltftvooda1gkiIqfV1qmptwU4R_Vv2jFYo3g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP581746.RA9wKc17bltftvooda1gkiIqfV1qmptwU4R_Vv2jFYo3g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP581746.RA9wKc17bltftvooda1gkiIqfV1qmptwU4R_Vv2jFYo3g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP581746.RA9wKc17bltftvooda1gkiIqfV1qmptwU4R_Vv2jFYo3g130_provenance.
- NP581746.RA9wKc17bltftvooda1gkiIqfV1qmptwU4R_Vv2jFYo3g130_assertion wasGeneratedBy ECO_0000203 NP581746.RA9wKc17bltftvooda1gkiIqfV1qmptwU4R_Vv2jFYo3g130_provenance.
- NP581746.RA9wKc17bltftvooda1gkiIqfV1qmptwU4R_Vv2jFYo3g130_assertion wasDerivedFrom befree-20150227 NP581746.RA9wKc17bltftvooda1gkiIqfV1qmptwU4R_Vv2jFYo3g130_provenance.
- NP581746.RA9wKc17bltftvooda1gkiIqfV1qmptwU4R_Vv2jFYo3g130_assertion SIO_000772 10643003 NP581746.RA9wKc17bltftvooda1gkiIqfV1qmptwU4R_Vv2jFYo3g130_provenance.
- NP581746.RA9wKc17bltftvooda1gkiIqfV1qmptwU4R_Vv2jFYo3g130_assertion evidence source_evidence_literature NP581746.RA9wKc17bltftvooda1gkiIqfV1qmptwU4R_Vv2jFYo3g130_provenance.
- NP581746.RA9wKc17bltftvooda1gkiIqfV1qmptwU4R_Vv2jFYo3g130_assertion description "[Comparative genomic hybridization (CGH) revealed regions of gains and amplification in three locations, with gains of chromosome 7, amplification of 8q24 (corresponding to the MYCC locus) and gains of the long arm of chromosome 17 (suggestive of isochromosome 17q).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581746.RA9wKc17bltftvooda1gkiIqfV1qmptwU4R_Vv2jFYo3g130_provenance.