Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP675997.RA9Oj7CoMiwZaZ1iGwx3duiKU5fFUri8lKS2cmY3Nel08130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP675997.RA9Oj7CoMiwZaZ1iGwx3duiKU5fFUri8lKS2cmY3Nel08130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP675997.RA9Oj7CoMiwZaZ1iGwx3duiKU5fFUri8lKS2cmY3Nel08130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP675997.RA9Oj7CoMiwZaZ1iGwx3duiKU5fFUri8lKS2cmY3Nel08130_provenance.
- NP675997.RA9Oj7CoMiwZaZ1iGwx3duiKU5fFUri8lKS2cmY3Nel08130_assertion description "[The five most prevalent diagnoses were Fanconi anemia (FA), Shwachman-Diamond syndrome (SDS), Diamond-Blackfan anemia (DBA), dyskeratosis congenita (DKC), and Kostmann's neutropenia (KS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP675997.RA9Oj7CoMiwZaZ1iGwx3duiKU5fFUri8lKS2cmY3Nel08130_provenance.
- NP675997.RA9Oj7CoMiwZaZ1iGwx3duiKU5fFUri8lKS2cmY3Nel08130_assertion evidence source_evidence_literature NP675997.RA9Oj7CoMiwZaZ1iGwx3duiKU5fFUri8lKS2cmY3Nel08130_provenance.
- NP675997.RA9Oj7CoMiwZaZ1iGwx3duiKU5fFUri8lKS2cmY3Nel08130_assertion SIO_000772 16676307 NP675997.RA9Oj7CoMiwZaZ1iGwx3duiKU5fFUri8lKS2cmY3Nel08130_provenance.
- NP675997.RA9Oj7CoMiwZaZ1iGwx3duiKU5fFUri8lKS2cmY3Nel08130_assertion wasDerivedFrom befree-20150227 NP675997.RA9Oj7CoMiwZaZ1iGwx3duiKU5fFUri8lKS2cmY3Nel08130_provenance.
- NP675997.RA9Oj7CoMiwZaZ1iGwx3duiKU5fFUri8lKS2cmY3Nel08130_assertion wasGeneratedBy ECO_0000203 NP675997.RA9Oj7CoMiwZaZ1iGwx3duiKU5fFUri8lKS2cmY3Nel08130_provenance.
- befree-20150227 importedOn "2015-02-27" NP675997.RA9Oj7CoMiwZaZ1iGwx3duiKU5fFUri8lKS2cmY3Nel08130_provenance.