Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP246633.RASxXQBi8cQsBeAdV2WRiqDHKBnZXhkiVJ0sUIixtmJAE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP246633.RASxXQBi8cQsBeAdV2WRiqDHKBnZXhkiVJ0sUIixtmJAE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP246633.RASxXQBi8cQsBeAdV2WRiqDHKBnZXhkiVJ0sUIixtmJAE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP246633.RASxXQBi8cQsBeAdV2WRiqDHKBnZXhkiVJ0sUIixtmJAE130_provenance.
- NP246633.RASxXQBi8cQsBeAdV2WRiqDHKBnZXhkiVJ0sUIixtmJAE130_assertion description "[DFNB3 maps within the common deletion region of Smith-Magenis syndrome (SMS), del(17)(p11.2p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP246633.RASxXQBi8cQsBeAdV2WRiqDHKBnZXhkiVJ0sUIixtmJAE130_provenance.
- NP246633.RASxXQBi8cQsBeAdV2WRiqDHKBnZXhkiVJ0sUIixtmJAE130_assertion evidence source_evidence_literature NP246633.RASxXQBi8cQsBeAdV2WRiqDHKBnZXhkiVJ0sUIixtmJAE130_provenance.
- NP246633.RASxXQBi8cQsBeAdV2WRiqDHKBnZXhkiVJ0sUIixtmJAE130_assertion SIO_000772 10049592 NP246633.RASxXQBi8cQsBeAdV2WRiqDHKBnZXhkiVJ0sUIixtmJAE130_provenance.
- NP246633.RASxXQBi8cQsBeAdV2WRiqDHKBnZXhkiVJ0sUIixtmJAE130_assertion wasDerivedFrom befree-2016 NP246633.RASxXQBi8cQsBeAdV2WRiqDHKBnZXhkiVJ0sUIixtmJAE130_provenance.
- NP246633.RASxXQBi8cQsBeAdV2WRiqDHKBnZXhkiVJ0sUIixtmJAE130_assertion wasGeneratedBy ECO_0000203 NP246633.RASxXQBi8cQsBeAdV2WRiqDHKBnZXhkiVJ0sUIixtmJAE130_provenance.
- befree-2016 importedOn "2016-02-19" NP246633.RASxXQBi8cQsBeAdV2WRiqDHKBnZXhkiVJ0sUIixtmJAE130_provenance.