Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1249508.RAxF6kfzSpWX2MB0SuxZE6T1wIE_GPg90Q3GTt4IpExbk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1249508.RAxF6kfzSpWX2MB0SuxZE6T1wIE_GPg90Q3GTt4IpExbk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1249508.RAxF6kfzSpWX2MB0SuxZE6T1wIE_GPg90Q3GTt4IpExbk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1249508.RAxF6kfzSpWX2MB0SuxZE6T1wIE_GPg90Q3GTt4IpExbk130_provenance.
- NP1249508.RAxF6kfzSpWX2MB0SuxZE6T1wIE_GPg90Q3GTt4IpExbk130_assertion description "[Dunnigan type familial partial lipodystrophy (FPLD2; OMIM#151660) is caused in most cases by the A-type lamin R482W mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249508.RAxF6kfzSpWX2MB0SuxZE6T1wIE_GPg90Q3GTt4IpExbk130_provenance.
- NP1249508.RAxF6kfzSpWX2MB0SuxZE6T1wIE_GPg90Q3GTt4IpExbk130_assertion evidence source_evidence_literature NP1249508.RAxF6kfzSpWX2MB0SuxZE6T1wIE_GPg90Q3GTt4IpExbk130_provenance.
- NP1249508.RAxF6kfzSpWX2MB0SuxZE6T1wIE_GPg90Q3GTt4IpExbk130_assertion SIO_000772 25524705 NP1249508.RAxF6kfzSpWX2MB0SuxZE6T1wIE_GPg90Q3GTt4IpExbk130_provenance.
- NP1249508.RAxF6kfzSpWX2MB0SuxZE6T1wIE_GPg90Q3GTt4IpExbk130_assertion wasDerivedFrom befree-2016 NP1249508.RAxF6kfzSpWX2MB0SuxZE6T1wIE_GPg90Q3GTt4IpExbk130_provenance.
- NP1249508.RAxF6kfzSpWX2MB0SuxZE6T1wIE_GPg90Q3GTt4IpExbk130_assertion wasGeneratedBy ECO_0000203 NP1249508.RAxF6kfzSpWX2MB0SuxZE6T1wIE_GPg90Q3GTt4IpExbk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1249508.RAxF6kfzSpWX2MB0SuxZE6T1wIE_GPg90Q3GTt4IpExbk130_provenance.