Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP887304.RAjKqRuqzG90JORUHXwJ_0K4s87LCZ0u8TT_D2B58UdqE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP887304.RAjKqRuqzG90JORUHXwJ_0K4s87LCZ0u8TT_D2B58UdqE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887304.RAjKqRuqzG90JORUHXwJ_0K4s87LCZ0u8TT_D2B58UdqE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887304.RAjKqRuqzG90JORUHXwJ_0K4s87LCZ0u8TT_D2B58UdqE130_provenance.
- NP887304.RAjKqRuqzG90JORUHXwJ_0K4s87LCZ0u8TT_D2B58UdqE130_assertion description "[ARX mutations cause a diverse spectrum of human disorders, ranging from severe brain and genital malformations to non-syndromic intellectual disability (ID).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887304.RAjKqRuqzG90JORUHXwJ_0K4s87LCZ0u8TT_D2B58UdqE130_provenance.
- NP887304.RAjKqRuqzG90JORUHXwJ_0K4s87LCZ0u8TT_D2B58UdqE130_assertion evidence source_evidence_literature NP887304.RAjKqRuqzG90JORUHXwJ_0K4s87LCZ0u8TT_D2B58UdqE130_provenance.
- NP887304.RAjKqRuqzG90JORUHXwJ_0K4s87LCZ0u8TT_D2B58UdqE130_assertion SIO_000772 21496008 NP887304.RAjKqRuqzG90JORUHXwJ_0K4s87LCZ0u8TT_D2B58UdqE130_provenance.
- NP887304.RAjKqRuqzG90JORUHXwJ_0K4s87LCZ0u8TT_D2B58UdqE130_assertion wasDerivedFrom befree-2016 NP887304.RAjKqRuqzG90JORUHXwJ_0K4s87LCZ0u8TT_D2B58UdqE130_provenance.
- NP887304.RAjKqRuqzG90JORUHXwJ_0K4s87LCZ0u8TT_D2B58UdqE130_assertion wasGeneratedBy ECO_0000203 NP887304.RAjKqRuqzG90JORUHXwJ_0K4s87LCZ0u8TT_D2B58UdqE130_provenance.
- befree-2016 importedOn "2016-02-19" NP887304.RAjKqRuqzG90JORUHXwJ_0K4s87LCZ0u8TT_D2B58UdqE130_provenance.