Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP869602.RAmQZwzKDJ0rwfy-aQ28aQWnd9rJwXblQLejHUMA-6NVU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP869602.RAmQZwzKDJ0rwfy-aQ28aQWnd9rJwXblQLejHUMA-6NVU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869602.RAmQZwzKDJ0rwfy-aQ28aQWnd9rJwXblQLejHUMA-6NVU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869602.RAmQZwzKDJ0rwfy-aQ28aQWnd9rJwXblQLejHUMA-6NVU130_provenance.
- NP869602.RAmQZwzKDJ0rwfy-aQ28aQWnd9rJwXblQLejHUMA-6NVU130_assertion description "[We searched for SLC35D1 mutations in five families with SBD and 15 patients with other SSDD group diseases, including achodrogenesis type 1A, spondylometaphyseal dysplasia Sedaghatian type and fibrochondrogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869602.RAmQZwzKDJ0rwfy-aQ28aQWnd9rJwXblQLejHUMA-6NVU130_provenance.
- NP869602.RAmQZwzKDJ0rwfy-aQ28aQWnd9rJwXblQLejHUMA-6NVU130_assertion evidence source_evidence_literature NP869602.RAmQZwzKDJ0rwfy-aQ28aQWnd9rJwXblQLejHUMA-6NVU130_provenance.
- NP869602.RAmQZwzKDJ0rwfy-aQ28aQWnd9rJwXblQLejHUMA-6NVU130_assertion SIO_000772 19508970 NP869602.RAmQZwzKDJ0rwfy-aQ28aQWnd9rJwXblQLejHUMA-6NVU130_provenance.
- NP869602.RAmQZwzKDJ0rwfy-aQ28aQWnd9rJwXblQLejHUMA-6NVU130_assertion wasDerivedFrom befree-20150227 NP869602.RAmQZwzKDJ0rwfy-aQ28aQWnd9rJwXblQLejHUMA-6NVU130_provenance.
- NP869602.RAmQZwzKDJ0rwfy-aQ28aQWnd9rJwXblQLejHUMA-6NVU130_assertion wasGeneratedBy ECO_0000203 NP869602.RAmQZwzKDJ0rwfy-aQ28aQWnd9rJwXblQLejHUMA-6NVU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP869602.RAmQZwzKDJ0rwfy-aQ28aQWnd9rJwXblQLejHUMA-6NVU130_provenance.