Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP921291.RACmRCPZZB27RMJ5flPUqgwbppiYJQIBBW5ixSAcxvjgU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP921291.RACmRCPZZB27RMJ5flPUqgwbppiYJQIBBW5ixSAcxvjgU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP921291.RACmRCPZZB27RMJ5flPUqgwbppiYJQIBBW5ixSAcxvjgU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP921291.RACmRCPZZB27RMJ5flPUqgwbppiYJQIBBW5ixSAcxvjgU130_provenance.
- NP921291.RACmRCPZZB27RMJ5flPUqgwbppiYJQIBBW5ixSAcxvjgU130_assertion description "[Our finding expands the spectrum of cataract phenotypes caused by the Q155X mutation of CRYBB2, confirms the phenotypic heterogeneity of this mutation and suggests the mechanism that influences the congenital cataract formation in different ethnic backgrounds.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921291.RACmRCPZZB27RMJ5flPUqgwbppiYJQIBBW5ixSAcxvjgU130_provenance.
- NP921291.RACmRCPZZB27RMJ5flPUqgwbppiYJQIBBW5ixSAcxvjgU130_assertion evidence source_evidence_literature NP921291.RACmRCPZZB27RMJ5flPUqgwbppiYJQIBBW5ixSAcxvjgU130_provenance.
- NP921291.RACmRCPZZB27RMJ5flPUqgwbppiYJQIBBW5ixSAcxvjgU130_assertion SIO_000772 16179907 NP921291.RACmRCPZZB27RMJ5flPUqgwbppiYJQIBBW5ixSAcxvjgU130_provenance.
- NP921291.RACmRCPZZB27RMJ5flPUqgwbppiYJQIBBW5ixSAcxvjgU130_assertion wasDerivedFrom befree-20140225 NP921291.RACmRCPZZB27RMJ5flPUqgwbppiYJQIBBW5ixSAcxvjgU130_provenance.
- NP921291.RACmRCPZZB27RMJ5flPUqgwbppiYJQIBBW5ixSAcxvjgU130_assertion wasGeneratedBy ECO_0000203 NP921291.RACmRCPZZB27RMJ5flPUqgwbppiYJQIBBW5ixSAcxvjgU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP921291.RACmRCPZZB27RMJ5flPUqgwbppiYJQIBBW5ixSAcxvjgU130_provenance.