Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1116533.RAEwDVj890L789AAP-e9cF0tiWq1td5IE8ZfiLSpxWlgc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1116533.RAEwDVj890L789AAP-e9cF0tiWq1td5IE8ZfiLSpxWlgc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1116533.RAEwDVj890L789AAP-e9cF0tiWq1td5IE8ZfiLSpxWlgc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1116533.RAEwDVj890L789AAP-e9cF0tiWq1td5IE8ZfiLSpxWlgc130_provenance.
- NP1116533.RAEwDVj890L789AAP-e9cF0tiWq1td5IE8ZfiLSpxWlgc130_assertion description "[GDF5 is a susceptibility gene for osteoarthritis (OA) and mutations in GDF5 are associated with a wide variety of skeletal malformations ranging from complex syndromes such as acromesomelic chondrodysplasias to isolated forms of brachydactylies or multiple synostoses syndrome 2 (SYNS2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1116533.RAEwDVj890L789AAP-e9cF0tiWq1td5IE8ZfiLSpxWlgc130_provenance.
- NP1116533.RAEwDVj890L789AAP-e9cF0tiWq1td5IE8ZfiLSpxWlgc130_assertion evidence source_evidence_literature NP1116533.RAEwDVj890L789AAP-e9cF0tiWq1td5IE8ZfiLSpxWlgc130_provenance.
- NP1116533.RAEwDVj890L789AAP-e9cF0tiWq1td5IE8ZfiLSpxWlgc130_assertion SIO_000772 24098149 NP1116533.RAEwDVj890L789AAP-e9cF0tiWq1td5IE8ZfiLSpxWlgc130_provenance.
- NP1116533.RAEwDVj890L789AAP-e9cF0tiWq1td5IE8ZfiLSpxWlgc130_assertion wasDerivedFrom befree-2016 NP1116533.RAEwDVj890L789AAP-e9cF0tiWq1td5IE8ZfiLSpxWlgc130_provenance.
- NP1116533.RAEwDVj890L789AAP-e9cF0tiWq1td5IE8ZfiLSpxWlgc130_assertion wasGeneratedBy ECO_0000203 NP1116533.RAEwDVj890L789AAP-e9cF0tiWq1td5IE8ZfiLSpxWlgc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1116533.RAEwDVj890L789AAP-e9cF0tiWq1td5IE8ZfiLSpxWlgc130_provenance.