Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP396739.RAwa54as7_w0pZ8qsjqkZ1S8c1UYkn9DCNi0BJKV25sBs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP396739.RAwa54as7_w0pZ8qsjqkZ1S8c1UYkn9DCNi0BJKV25sBs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP396739.RAwa54as7_w0pZ8qsjqkZ1S8c1UYkn9DCNi0BJKV25sBs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP396739.RAwa54as7_w0pZ8qsjqkZ1S8c1UYkn9DCNi0BJKV25sBs130_provenance.
- befree-2016 importedOn "2016-02-19" NP396739.RAwa54as7_w0pZ8qsjqkZ1S8c1UYkn9DCNi0BJKV25sBs130_provenance.
- NP396739.RAwa54as7_w0pZ8qsjqkZ1S8c1UYkn9DCNi0BJKV25sBs130_assertion wasGeneratedBy ECO_0000203 NP396739.RAwa54as7_w0pZ8qsjqkZ1S8c1UYkn9DCNi0BJKV25sBs130_provenance.
- NP396739.RAwa54as7_w0pZ8qsjqkZ1S8c1UYkn9DCNi0BJKV25sBs130_assertion wasDerivedFrom befree-2016 NP396739.RAwa54as7_w0pZ8qsjqkZ1S8c1UYkn9DCNi0BJKV25sBs130_provenance.
- NP396739.RAwa54as7_w0pZ8qsjqkZ1S8c1UYkn9DCNi0BJKV25sBs130_assertion SIO_000772 12783988 NP396739.RAwa54as7_w0pZ8qsjqkZ1S8c1UYkn9DCNi0BJKV25sBs130_provenance.
- NP396739.RAwa54as7_w0pZ8qsjqkZ1S8c1UYkn9DCNi0BJKV25sBs130_assertion evidence source_evidence_literature NP396739.RAwa54as7_w0pZ8qsjqkZ1S8c1UYkn9DCNi0BJKV25sBs130_provenance.
- NP396739.RAwa54as7_w0pZ8qsjqkZ1S8c1UYkn9DCNi0BJKV25sBs130_assertion description "[The novel hypothesis suggested by the data is that EDMD/CMD1A mutations in the tail domain of lamin A/C work by direct impairment of emerin interaction, whereas mutations in the rod region cause defective lamina assembly that might or might not impair emerin capture at the nuclear rim.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP396739.RAwa54as7_w0pZ8qsjqkZ1S8c1UYkn9DCNi0BJKV25sBs130_provenance.