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- source_evidence_literature type ECO_0000212 NP302230.RA9M5sqmllyecD6-vWnv7LKvHEPj16n1hesaSV9s8Cvpc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP302230.RA9M5sqmllyecD6-vWnv7LKvHEPj16n1hesaSV9s8Cvpc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP302230.RA9M5sqmllyecD6-vWnv7LKvHEPj16n1hesaSV9s8Cvpc130_provenance.
- NP302230.RA9M5sqmllyecD6-vWnv7LKvHEPj16n1hesaSV9s8Cvpc130_assertion description "[However, the absence of MSX2 mutations in some of the FPP patients analysed and the presence of FPP associated with chromosome 11p deletions in DEFECT 11 (OMIM 601224) patients or associated with Saethre-Chotzen syndrome suggests genetic heterogeneity for this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP302230.RA9M5sqmllyecD6-vWnv7LKvHEPj16n1hesaSV9s8Cvpc130_provenance.
- NP302230.RA9M5sqmllyecD6-vWnv7LKvHEPj16n1hesaSV9s8Cvpc130_assertion evidence source_evidence_literature NP302230.RA9M5sqmllyecD6-vWnv7LKvHEPj16n1hesaSV9s8Cvpc130_provenance.
- NP302230.RA9M5sqmllyecD6-vWnv7LKvHEPj16n1hesaSV9s8Cvpc130_assertion SIO_000772 11106354 NP302230.RA9M5sqmllyecD6-vWnv7LKvHEPj16n1hesaSV9s8Cvpc130_provenance.
- NP302230.RA9M5sqmllyecD6-vWnv7LKvHEPj16n1hesaSV9s8Cvpc130_assertion wasDerivedFrom befree-2016 NP302230.RA9M5sqmllyecD6-vWnv7LKvHEPj16n1hesaSV9s8Cvpc130_provenance.
- NP302230.RA9M5sqmllyecD6-vWnv7LKvHEPj16n1hesaSV9s8Cvpc130_assertion wasGeneratedBy ECO_0000203 NP302230.RA9M5sqmllyecD6-vWnv7LKvHEPj16n1hesaSV9s8Cvpc130_provenance.
- befree-2016 importedOn "2016-02-19" NP302230.RA9M5sqmllyecD6-vWnv7LKvHEPj16n1hesaSV9s8Cvpc130_provenance.