Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP218814.RAyM_VwfjdPKX6-gz4AO8VLtZmCl6k7cG_icAysU83cMA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP218814.RAyM_VwfjdPKX6-gz4AO8VLtZmCl6k7cG_icAysU83cMA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP218814.RAyM_VwfjdPKX6-gz4AO8VLtZmCl6k7cG_icAysU83cMA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP218814.RAyM_VwfjdPKX6-gz4AO8VLtZmCl6k7cG_icAysU83cMA130_provenance.
- NP218814.RAyM_VwfjdPKX6-gz4AO8VLtZmCl6k7cG_icAysU83cMA130_assertion wasGeneratedBy ECO_0000203 NP218814.RAyM_VwfjdPKX6-gz4AO8VLtZmCl6k7cG_icAysU83cMA130_provenance.
- NP218814.RAyM_VwfjdPKX6-gz4AO8VLtZmCl6k7cG_icAysU83cMA130_assertion wasDerivedFrom befree-20140225 NP218814.RAyM_VwfjdPKX6-gz4AO8VLtZmCl6k7cG_icAysU83cMA130_provenance.
- NP218814.RAyM_VwfjdPKX6-gz4AO8VLtZmCl6k7cG_icAysU83cMA130_assertion SIO_000772 17434305 NP218814.RAyM_VwfjdPKX6-gz4AO8VLtZmCl6k7cG_icAysU83cMA130_provenance.
- NP218814.RAyM_VwfjdPKX6-gz4AO8VLtZmCl6k7cG_icAysU83cMA130_assertion evidence source_evidence_literature NP218814.RAyM_VwfjdPKX6-gz4AO8VLtZmCl6k7cG_icAysU83cMA130_provenance.
- NP218814.RAyM_VwfjdPKX6-gz4AO8VLtZmCl6k7cG_icAysU83cMA130_assertion description "[Mutations in embryonic MyHC (MYH3) and perinatal MyHC (MYH8), which are myosin isoforms expressed during muscle development, are associated with distal arthrogryposis syndromes with no or minor muscle weakness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218814.RAyM_VwfjdPKX6-gz4AO8VLtZmCl6k7cG_icAysU83cMA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP218814.RAyM_VwfjdPKX6-gz4AO8VLtZmCl6k7cG_icAysU83cMA130_provenance.