Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1249508.RAxF6kfzSpWX2MB0SuxZE6T1wIE_GPg90Q3GTt4IpExbk130_assertion> ?p ?o ?g. }
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- NP1249508.RAxF6kfzSpWX2MB0SuxZE6T1wIE_GPg90Q3GTt4IpExbk130_assertion type Assertion NP1249508.RAxF6kfzSpWX2MB0SuxZE6T1wIE_GPg90Q3GTt4IpExbk130_head.
- 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.