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- source_evidence_literature type ECO_0000212 NP388468.RA51ajVl-1Md9WsT76foIYzU2icIOw9khMXu2m13xqg5c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP388468.RA51ajVl-1Md9WsT76foIYzU2icIOw9khMXu2m13xqg5c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP388468.RA51ajVl-1Md9WsT76foIYzU2icIOw9khMXu2m13xqg5c130_provenance.
- NP388468.RA51ajVl-1Md9WsT76foIYzU2icIOw9khMXu2m13xqg5c130_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." NP388468.RA51ajVl-1Md9WsT76foIYzU2icIOw9khMXu2m13xqg5c130_provenance.
- NP388468.RA51ajVl-1Md9WsT76foIYzU2icIOw9khMXu2m13xqg5c130_assertion evidence source_evidence_literature NP388468.RA51ajVl-1Md9WsT76foIYzU2icIOw9khMXu2m13xqg5c130_provenance.
- NP388468.RA51ajVl-1Md9WsT76foIYzU2icIOw9khMXu2m13xqg5c130_assertion SIO_000772 22116208 NP388468.RA51ajVl-1Md9WsT76foIYzU2icIOw9khMXu2m13xqg5c130_provenance.
- NP388468.RA51ajVl-1Md9WsT76foIYzU2icIOw9khMXu2m13xqg5c130_assertion wasDerivedFrom befree-20150227 NP388468.RA51ajVl-1Md9WsT76foIYzU2icIOw9khMXu2m13xqg5c130_provenance.
- NP388468.RA51ajVl-1Md9WsT76foIYzU2icIOw9khMXu2m13xqg5c130_assertion wasGeneratedBy ECO_0000203 NP388468.RA51ajVl-1Md9WsT76foIYzU2icIOw9khMXu2m13xqg5c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP388468.RA51ajVl-1Md9WsT76foIYzU2icIOw9khMXu2m13xqg5c130_provenance.