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- source_evidence_literature type ECO_0000212 NP395928.RAew86lnKjOQmrT0tPThZIFzWzuy33OfwW-pD2dGeURC4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP395928.RAew86lnKjOQmrT0tPThZIFzWzuy33OfwW-pD2dGeURC4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP395928.RAew86lnKjOQmrT0tPThZIFzWzuy33OfwW-pD2dGeURC4130_provenance.
- NP395928.RAew86lnKjOQmrT0tPThZIFzWzuy33OfwW-pD2dGeURC4130_assertion description "[Dominant FBN1 mutations cause IEL or syndromic ectopia lentis (Marfan syndrome and Weill-Marchesani syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP395928.RAew86lnKjOQmrT0tPThZIFzWzuy33OfwW-pD2dGeURC4130_provenance.
- NP395928.RAew86lnKjOQmrT0tPThZIFzWzuy33OfwW-pD2dGeURC4130_assertion evidence source_evidence_literature NP395928.RAew86lnKjOQmrT0tPThZIFzWzuy33OfwW-pD2dGeURC4130_provenance.
- NP395928.RAew86lnKjOQmrT0tPThZIFzWzuy33OfwW-pD2dGeURC4130_assertion SIO_000772 21989719 NP395928.RAew86lnKjOQmrT0tPThZIFzWzuy33OfwW-pD2dGeURC4130_provenance.
- NP395928.RAew86lnKjOQmrT0tPThZIFzWzuy33OfwW-pD2dGeURC4130_assertion wasDerivedFrom befree-20150227 NP395928.RAew86lnKjOQmrT0tPThZIFzWzuy33OfwW-pD2dGeURC4130_provenance.
- NP395928.RAew86lnKjOQmrT0tPThZIFzWzuy33OfwW-pD2dGeURC4130_assertion wasGeneratedBy ECO_0000203 NP395928.RAew86lnKjOQmrT0tPThZIFzWzuy33OfwW-pD2dGeURC4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP395928.RAew86lnKjOQmrT0tPThZIFzWzuy33OfwW-pD2dGeURC4130_provenance.