Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP156611.RALoXEDJn-f52IhbU3R2xX-H9-F4gxjo3dPMIN2KZ80gk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP156611.RALoXEDJn-f52IhbU3R2xX-H9-F4gxjo3dPMIN2KZ80gk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP156611.RALoXEDJn-f52IhbU3R2xX-H9-F4gxjo3dPMIN2KZ80gk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP156611.RALoXEDJn-f52IhbU3R2xX-H9-F4gxjo3dPMIN2KZ80gk130_provenance.
- NP156611.RALoXEDJn-f52IhbU3R2xX-H9-F4gxjo3dPMIN2KZ80gk130_assertion wasGeneratedBy ECO_0000203 NP156611.RALoXEDJn-f52IhbU3R2xX-H9-F4gxjo3dPMIN2KZ80gk130_provenance.
- NP156611.RALoXEDJn-f52IhbU3R2xX-H9-F4gxjo3dPMIN2KZ80gk130_assertion wasDerivedFrom befree-20140225 NP156611.RALoXEDJn-f52IhbU3R2xX-H9-F4gxjo3dPMIN2KZ80gk130_provenance.
- NP156611.RALoXEDJn-f52IhbU3R2xX-H9-F4gxjo3dPMIN2KZ80gk130_assertion SIO_000772 21236492 NP156611.RALoXEDJn-f52IhbU3R2xX-H9-F4gxjo3dPMIN2KZ80gk130_provenance.
- NP156611.RALoXEDJn-f52IhbU3R2xX-H9-F4gxjo3dPMIN2KZ80gk130_assertion evidence source_evidence_literature NP156611.RALoXEDJn-f52IhbU3R2xX-H9-F4gxjo3dPMIN2KZ80gk130_provenance.
- NP156611.RALoXEDJn-f52IhbU3R2xX-H9-F4gxjo3dPMIN2KZ80gk130_assertion description "[A novel mutation of LAMB2 in a multigenerational mennonite family reveals a new phenotypic variant of Pierson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP156611.RALoXEDJn-f52IhbU3R2xX-H9-F4gxjo3dPMIN2KZ80gk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP156611.RALoXEDJn-f52IhbU3R2xX-H9-F4gxjo3dPMIN2KZ80gk130_provenance.