Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP532695.RAQ1uHVfw5VXsZGXcOfpGX2ajzjAUFf6XyS7NREw4g6mg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP532695.RAQ1uHVfw5VXsZGXcOfpGX2ajzjAUFf6XyS7NREw4g6mg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP532695.RAQ1uHVfw5VXsZGXcOfpGX2ajzjAUFf6XyS7NREw4g6mg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP532695.RAQ1uHVfw5VXsZGXcOfpGX2ajzjAUFf6XyS7NREw4g6mg130_provenance.
- NP532695.RAQ1uHVfw5VXsZGXcOfpGX2ajzjAUFf6XyS7NREw4g6mg130_assertion wasGeneratedBy ECO_0000203 NP532695.RAQ1uHVfw5VXsZGXcOfpGX2ajzjAUFf6XyS7NREw4g6mg130_provenance.
- NP532695.RAQ1uHVfw5VXsZGXcOfpGX2ajzjAUFf6XyS7NREw4g6mg130_assertion wasDerivedFrom befree-20140225 NP532695.RAQ1uHVfw5VXsZGXcOfpGX2ajzjAUFf6XyS7NREw4g6mg130_provenance.
- NP532695.RAQ1uHVfw5VXsZGXcOfpGX2ajzjAUFf6XyS7NREw4g6mg130_assertion SIO_000772 24140113 NP532695.RAQ1uHVfw5VXsZGXcOfpGX2ajzjAUFf6XyS7NREw4g6mg130_provenance.
- NP532695.RAQ1uHVfw5VXsZGXcOfpGX2ajzjAUFf6XyS7NREw4g6mg130_assertion evidence source_evidence_literature NP532695.RAQ1uHVfw5VXsZGXcOfpGX2ajzjAUFf6XyS7NREw4g6mg130_provenance.
- NP532695.RAQ1uHVfw5VXsZGXcOfpGX2ajzjAUFf6XyS7NREw4g6mg130_assertion description "[All six IFT-A components and their motor protein, DYNC2H1, have been linked to human skeletal ciliopathies, including asphyxiating thoracic dystrophy (ATD; also known as Jeune syndrome), Sensenbrenner syndrome, and Mainzer-Saldino syndrome (MZSDS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532695.RAQ1uHVfw5VXsZGXcOfpGX2ajzjAUFf6XyS7NREw4g6mg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP532695.RAQ1uHVfw5VXsZGXcOfpGX2ajzjAUFf6XyS7NREw4g6mg130_provenance.