Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP290708.RAa4qhwQW8svrHYSjSOWPtDYkYo_l3qaCZABsP5W89Sp0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP290708.RAa4qhwQW8svrHYSjSOWPtDYkYo_l3qaCZABsP5W89Sp0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP290708.RAa4qhwQW8svrHYSjSOWPtDYkYo_l3qaCZABsP5W89Sp0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP290708.RAa4qhwQW8svrHYSjSOWPtDYkYo_l3qaCZABsP5W89Sp0130_provenance.
- NP290708.RAa4qhwQW8svrHYSjSOWPtDYkYo_l3qaCZABsP5W89Sp0130_assertion description "[Here, we described that homozygous mutations in EXT1/EXT2, which are causative for osteochondroma formation, are likely to affect terminal chondrocyte differentiation and vascularisation in the osteocartilaginous interface.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP290708.RAa4qhwQW8svrHYSjSOWPtDYkYo_l3qaCZABsP5W89Sp0130_provenance.
- NP290708.RAa4qhwQW8svrHYSjSOWPtDYkYo_l3qaCZABsP5W89Sp0130_assertion evidence source_evidence_literature NP290708.RAa4qhwQW8svrHYSjSOWPtDYkYo_l3qaCZABsP5W89Sp0130_provenance.
- NP290708.RAa4qhwQW8svrHYSjSOWPtDYkYo_l3qaCZABsP5W89Sp0130_assertion SIO_000772 22116208 NP290708.RAa4qhwQW8svrHYSjSOWPtDYkYo_l3qaCZABsP5W89Sp0130_provenance.
- NP290708.RAa4qhwQW8svrHYSjSOWPtDYkYo_l3qaCZABsP5W89Sp0130_assertion wasDerivedFrom befree-20140225 NP290708.RAa4qhwQW8svrHYSjSOWPtDYkYo_l3qaCZABsP5W89Sp0130_provenance.
- NP290708.RAa4qhwQW8svrHYSjSOWPtDYkYo_l3qaCZABsP5W89Sp0130_assertion wasGeneratedBy ECO_0000203 NP290708.RAa4qhwQW8svrHYSjSOWPtDYkYo_l3qaCZABsP5W89Sp0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP290708.RAa4qhwQW8svrHYSjSOWPtDYkYo_l3qaCZABsP5W89Sp0130_provenance.