Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP317525.RAIEVOc-vXaMdZwkLcfQIueHvuMnV2DTbXD45HjCbUy3w130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP317525.RAIEVOc-vXaMdZwkLcfQIueHvuMnV2DTbXD45HjCbUy3w130_assertion type Assertion NP317525.RAIEVOc-vXaMdZwkLcfQIueHvuMnV2DTbXD45HjCbUy3w130_head.
- NP317525.RAIEVOc-vXaMdZwkLcfQIueHvuMnV2DTbXD45HjCbUy3w130_assertion description "[PROMM (proximal myotonic myopathy) and DM2 (myotonic dystrophy Type 2) are autosomal dominant multisystem disorders that have both been linked to chromosome 3q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317525.RAIEVOc-vXaMdZwkLcfQIueHvuMnV2DTbXD45HjCbUy3w130_provenance.
- NP317525.RAIEVOc-vXaMdZwkLcfQIueHvuMnV2DTbXD45HjCbUy3w130_assertion evidence source_evidence_literature NP317525.RAIEVOc-vXaMdZwkLcfQIueHvuMnV2DTbXD45HjCbUy3w130_provenance.
- NP317525.RAIEVOc-vXaMdZwkLcfQIueHvuMnV2DTbXD45HjCbUy3w130_assertion SIO_000772 15261229 NP317525.RAIEVOc-vXaMdZwkLcfQIueHvuMnV2DTbXD45HjCbUy3w130_provenance.
- NP317525.RAIEVOc-vXaMdZwkLcfQIueHvuMnV2DTbXD45HjCbUy3w130_assertion wasDerivedFrom befree-20140225 NP317525.RAIEVOc-vXaMdZwkLcfQIueHvuMnV2DTbXD45HjCbUy3w130_provenance.
- NP317525.RAIEVOc-vXaMdZwkLcfQIueHvuMnV2DTbXD45HjCbUy3w130_assertion wasGeneratedBy ECO_0000203 NP317525.RAIEVOc-vXaMdZwkLcfQIueHvuMnV2DTbXD45HjCbUy3w130_provenance.