Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP319620.RAfAe3dQumQo6Mi1Gxln0xBNvQVSheTLfRX-XNkIGIYTE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP319620.RAfAe3dQumQo6Mi1Gxln0xBNvQVSheTLfRX-XNkIGIYTE130_assertion type Assertion NP319620.RAfAe3dQumQo6Mi1Gxln0xBNvQVSheTLfRX-XNkIGIYTE130_head.
- NP319620.RAfAe3dQumQo6Mi1Gxln0xBNvQVSheTLfRX-XNkIGIYTE130_assertion description "[Based on the previous finding that mutations in COL3A1 cause type IV EDS, our study indicates a possible common pathological pathway linking connective tissue diseases and brain malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319620.RAfAe3dQumQo6Mi1Gxln0xBNvQVSheTLfRX-XNkIGIYTE130_provenance.
- NP319620.RAfAe3dQumQo6Mi1Gxln0xBNvQVSheTLfRX-XNkIGIYTE130_assertion evidence source_evidence_literature NP319620.RAfAe3dQumQo6Mi1Gxln0xBNvQVSheTLfRX-XNkIGIYTE130_provenance.
- NP319620.RAfAe3dQumQo6Mi1Gxln0xBNvQVSheTLfRX-XNkIGIYTE130_assertion SIO_000772 22235340 NP319620.RAfAe3dQumQo6Mi1Gxln0xBNvQVSheTLfRX-XNkIGIYTE130_provenance.
- NP319620.RAfAe3dQumQo6Mi1Gxln0xBNvQVSheTLfRX-XNkIGIYTE130_assertion wasDerivedFrom befree-20150227 NP319620.RAfAe3dQumQo6Mi1Gxln0xBNvQVSheTLfRX-XNkIGIYTE130_provenance.
- NP319620.RAfAe3dQumQo6Mi1Gxln0xBNvQVSheTLfRX-XNkIGIYTE130_assertion wasGeneratedBy ECO_0000203 NP319620.RAfAe3dQumQo6Mi1Gxln0xBNvQVSheTLfRX-XNkIGIYTE130_provenance.