Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP444101.RAp7n_T_egqYnSaCNbSvMk5akOqFAHIyIaq0HGv2RWuQU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP444101.RAp7n_T_egqYnSaCNbSvMk5akOqFAHIyIaq0HGv2RWuQU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP444101.RAp7n_T_egqYnSaCNbSvMk5akOqFAHIyIaq0HGv2RWuQU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP444101.RAp7n_T_egqYnSaCNbSvMk5akOqFAHIyIaq0HGv2RWuQU130_provenance.
- NP444101.RAp7n_T_egqYnSaCNbSvMk5akOqFAHIyIaq0HGv2RWuQU130_assertion description "[Mutations at the alpha-globin locus are the most common class of mutations in humans, with deletion of all four adult alpha-globin genes resulting in the perinatal lethal condition haemoglobin Barts hydrops fetalis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444101.RAp7n_T_egqYnSaCNbSvMk5akOqFAHIyIaq0HGv2RWuQU130_provenance.
- NP444101.RAp7n_T_egqYnSaCNbSvMk5akOqFAHIyIaq0HGv2RWuQU130_assertion evidence source_evidence_literature NP444101.RAp7n_T_egqYnSaCNbSvMk5akOqFAHIyIaq0HGv2RWuQU130_provenance.
- NP444101.RAp7n_T_egqYnSaCNbSvMk5akOqFAHIyIaq0HGv2RWuQU130_assertion SIO_000772 7550311 NP444101.RAp7n_T_egqYnSaCNbSvMk5akOqFAHIyIaq0HGv2RWuQU130_provenance.
- NP444101.RAp7n_T_egqYnSaCNbSvMk5akOqFAHIyIaq0HGv2RWuQU130_assertion wasDerivedFrom befree-20150227 NP444101.RAp7n_T_egqYnSaCNbSvMk5akOqFAHIyIaq0HGv2RWuQU130_provenance.
- NP444101.RAp7n_T_egqYnSaCNbSvMk5akOqFAHIyIaq0HGv2RWuQU130_assertion wasGeneratedBy ECO_0000203 NP444101.RAp7n_T_egqYnSaCNbSvMk5akOqFAHIyIaq0HGv2RWuQU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP444101.RAp7n_T_egqYnSaCNbSvMk5akOqFAHIyIaq0HGv2RWuQU130_provenance.