Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP668107.RAmuX_LmOJJEv5h3O0C5UBKPPZKpL2w9OCc8lN8f4VmUc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP668107.RAmuX_LmOJJEv5h3O0C5UBKPPZKpL2w9OCc8lN8f4VmUc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668107.RAmuX_LmOJJEv5h3O0C5UBKPPZKpL2w9OCc8lN8f4VmUc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668107.RAmuX_LmOJJEv5h3O0C5UBKPPZKpL2w9OCc8lN8f4VmUc130_provenance.
- NP668107.RAmuX_LmOJJEv5h3O0C5UBKPPZKpL2w9OCc8lN8f4VmUc130_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." NP668107.RAmuX_LmOJJEv5h3O0C5UBKPPZKpL2w9OCc8lN8f4VmUc130_provenance.
- NP668107.RAmuX_LmOJJEv5h3O0C5UBKPPZKpL2w9OCc8lN8f4VmUc130_assertion evidence source_evidence_literature NP668107.RAmuX_LmOJJEv5h3O0C5UBKPPZKpL2w9OCc8lN8f4VmUc130_provenance.
- NP668107.RAmuX_LmOJJEv5h3O0C5UBKPPZKpL2w9OCc8lN8f4VmUc130_assertion SIO_000772 7550311 NP668107.RAmuX_LmOJJEv5h3O0C5UBKPPZKpL2w9OCc8lN8f4VmUc130_provenance.
- NP668107.RAmuX_LmOJJEv5h3O0C5UBKPPZKpL2w9OCc8lN8f4VmUc130_assertion wasDerivedFrom befree-20140225 NP668107.RAmuX_LmOJJEv5h3O0C5UBKPPZKpL2w9OCc8lN8f4VmUc130_provenance.
- NP668107.RAmuX_LmOJJEv5h3O0C5UBKPPZKpL2w9OCc8lN8f4VmUc130_assertion wasGeneratedBy ECO_0000203 NP668107.RAmuX_LmOJJEv5h3O0C5UBKPPZKpL2w9OCc8lN8f4VmUc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP668107.RAmuX_LmOJJEv5h3O0C5UBKPPZKpL2w9OCc8lN8f4VmUc130_provenance.