Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP546888.RANL8sEiTwKmwysSD5UeQjTJMQuNO68xCT_ppRZSu8ylg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP546888.RANL8sEiTwKmwysSD5UeQjTJMQuNO68xCT_ppRZSu8ylg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP546888.RANL8sEiTwKmwysSD5UeQjTJMQuNO68xCT_ppRZSu8ylg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP546888.RANL8sEiTwKmwysSD5UeQjTJMQuNO68xCT_ppRZSu8ylg130_provenance.
- NP546888.RANL8sEiTwKmwysSD5UeQjTJMQuNO68xCT_ppRZSu8ylg130_assertion description "[Patients carrying the T(303)M mutation in the gene for matrilin-3 express a form of HOA that is radiologically indistinguishable from idiopathic HOA in individual patients but they have more severe thumb-base involvement, particularly in the STT joint.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP546888.RANL8sEiTwKmwysSD5UeQjTJMQuNO68xCT_ppRZSu8ylg130_provenance.
- NP546888.RANL8sEiTwKmwysSD5UeQjTJMQuNO68xCT_ppRZSu8ylg130_assertion evidence source_evidence_literature NP546888.RANL8sEiTwKmwysSD5UeQjTJMQuNO68xCT_ppRZSu8ylg130_provenance.
- NP546888.RANL8sEiTwKmwysSD5UeQjTJMQuNO68xCT_ppRZSu8ylg130_assertion SIO_000772 16641049 NP546888.RANL8sEiTwKmwysSD5UeQjTJMQuNO68xCT_ppRZSu8ylg130_provenance.
- NP546888.RANL8sEiTwKmwysSD5UeQjTJMQuNO68xCT_ppRZSu8ylg130_assertion wasDerivedFrom befree-2016 NP546888.RANL8sEiTwKmwysSD5UeQjTJMQuNO68xCT_ppRZSu8ylg130_provenance.
- NP546888.RANL8sEiTwKmwysSD5UeQjTJMQuNO68xCT_ppRZSu8ylg130_assertion wasGeneratedBy ECO_0000203 NP546888.RANL8sEiTwKmwysSD5UeQjTJMQuNO68xCT_ppRZSu8ylg130_provenance.
- befree-2016 importedOn "2016-02-19" NP546888.RANL8sEiTwKmwysSD5UeQjTJMQuNO68xCT_ppRZSu8ylg130_provenance.