Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP849370.RAgfvPMUYnUU104odRvApyL1Uo5WItAyfeiXFTWDoA3l0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP849370.RAgfvPMUYnUU104odRvApyL1Uo5WItAyfeiXFTWDoA3l0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP849370.RAgfvPMUYnUU104odRvApyL1Uo5WItAyfeiXFTWDoA3l0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP849370.RAgfvPMUYnUU104odRvApyL1Uo5WItAyfeiXFTWDoA3l0130_provenance.
- NP849370.RAgfvPMUYnUU104odRvApyL1Uo5WItAyfeiXFTWDoA3l0130_assertion description "[The autosomal recessive skeletal dysplasia known as 'acromesomelic dysplasia, type Maroteaux' (AMDM) maps to an interval that contains NPR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP849370.RAgfvPMUYnUU104odRvApyL1Uo5WItAyfeiXFTWDoA3l0130_provenance.
- NP849370.RAgfvPMUYnUU104odRvApyL1Uo5WItAyfeiXFTWDoA3l0130_assertion evidence source_evidence_literature NP849370.RAgfvPMUYnUU104odRvApyL1Uo5WItAyfeiXFTWDoA3l0130_provenance.
- NP849370.RAgfvPMUYnUU104odRvApyL1Uo5WItAyfeiXFTWDoA3l0130_assertion SIO_000772 15146390 NP849370.RAgfvPMUYnUU104odRvApyL1Uo5WItAyfeiXFTWDoA3l0130_provenance.
- NP849370.RAgfvPMUYnUU104odRvApyL1Uo5WItAyfeiXFTWDoA3l0130_assertion wasDerivedFrom befree-20150227 NP849370.RAgfvPMUYnUU104odRvApyL1Uo5WItAyfeiXFTWDoA3l0130_provenance.
- NP849370.RAgfvPMUYnUU104odRvApyL1Uo5WItAyfeiXFTWDoA3l0130_assertion wasGeneratedBy ECO_0000203 NP849370.RAgfvPMUYnUU104odRvApyL1Uo5WItAyfeiXFTWDoA3l0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP849370.RAgfvPMUYnUU104odRvApyL1Uo5WItAyfeiXFTWDoA3l0130_provenance.