Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_provenance.
- NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_assertion description "[Mutations in human AHI1 underlie the autosomal recessive Joubert Syndrome with brain malformation and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_provenance.
- NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_assertion evidence source_evidence_literature NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_provenance.
- NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_assertion SIO_000772 16773125 NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_provenance.
- NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_assertion wasDerivedFrom befree-20150227 NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_provenance.
- NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_assertion wasGeneratedBy ECO_0000203 NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_provenance.