Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP257671.RAWBKx7mJ0Jybflclp70uLHvO4BoAHo5jf39EYkztLLC8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP257671.RAWBKx7mJ0Jybflclp70uLHvO4BoAHo5jf39EYkztLLC8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP257671.RAWBKx7mJ0Jybflclp70uLHvO4BoAHo5jf39EYkztLLC8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP257671.RAWBKx7mJ0Jybflclp70uLHvO4BoAHo5jf39EYkztLLC8130_provenance.
- NP257671.RAWBKx7mJ0Jybflclp70uLHvO4BoAHo5jf39EYkztLLC8130_assertion description "[Array-comparative genomic hybridisation (CGH) studies show universal genomic aberrations in both familial and sporadic breast cancer subtypes that may be selected in the breast tumour development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257671.RAWBKx7mJ0Jybflclp70uLHvO4BoAHo5jf39EYkztLLC8130_provenance.
- NP257671.RAWBKx7mJ0Jybflclp70uLHvO4BoAHo5jf39EYkztLLC8130_assertion evidence source_evidence_literature NP257671.RAWBKx7mJ0Jybflclp70uLHvO4BoAHo5jf39EYkztLLC8130_provenance.
- NP257671.RAWBKx7mJ0Jybflclp70uLHvO4BoAHo5jf39EYkztLLC8130_assertion SIO_000772 18596026 NP257671.RAWBKx7mJ0Jybflclp70uLHvO4BoAHo5jf39EYkztLLC8130_provenance.
- NP257671.RAWBKx7mJ0Jybflclp70uLHvO4BoAHo5jf39EYkztLLC8130_assertion wasDerivedFrom befree-20140225 NP257671.RAWBKx7mJ0Jybflclp70uLHvO4BoAHo5jf39EYkztLLC8130_provenance.
- NP257671.RAWBKx7mJ0Jybflclp70uLHvO4BoAHo5jf39EYkztLLC8130_assertion wasGeneratedBy ECO_0000203 NP257671.RAWBKx7mJ0Jybflclp70uLHvO4BoAHo5jf39EYkztLLC8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP257671.RAWBKx7mJ0Jybflclp70uLHvO4BoAHo5jf39EYkztLLC8130_provenance.