Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_provenance.
- NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_assertion description "[Determination of the sequence of the SNX10 gene is warranted in molecularly undefined patients with recessive 'pure' osteopetrosis of infancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_provenance.
- NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_assertion evidence source_evidence_literature NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_provenance.
- NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_assertion SIO_000772 22499339 NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_provenance.
- NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_assertion wasDerivedFrom befree-20140225 NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_provenance.
- NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_assertion wasGeneratedBy ECO_0000203 NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_provenance.