Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP409003.RAn56VcOe6TluIGd9BJC2ul7Ju_gxRogI-CL54RBB_ad4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP409003.RAn56VcOe6TluIGd9BJC2ul7Ju_gxRogI-CL54RBB_ad4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP409003.RAn56VcOe6TluIGd9BJC2ul7Ju_gxRogI-CL54RBB_ad4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP409003.RAn56VcOe6TluIGd9BJC2ul7Ju_gxRogI-CL54RBB_ad4130_provenance.
- NP409003.RAn56VcOe6TluIGd9BJC2ul7Ju_gxRogI-CL54RBB_ad4130_assertion description "[The ataxia telangiectasia mutated-Rad3 related (ATR)-Chk1 pathway is defective in Seckel syndrome, another microcephaly disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409003.RAn56VcOe6TluIGd9BJC2ul7Ju_gxRogI-CL54RBB_ad4130_provenance.
- NP409003.RAn56VcOe6TluIGd9BJC2ul7Ju_gxRogI-CL54RBB_ad4130_assertion evidence source_evidence_literature NP409003.RAn56VcOe6TluIGd9BJC2ul7Ju_gxRogI-CL54RBB_ad4130_provenance.
- NP409003.RAn56VcOe6TluIGd9BJC2ul7Ju_gxRogI-CL54RBB_ad4130_assertion SIO_000772 16217032 NP409003.RAn56VcOe6TluIGd9BJC2ul7Ju_gxRogI-CL54RBB_ad4130_provenance.
- NP409003.RAn56VcOe6TluIGd9BJC2ul7Ju_gxRogI-CL54RBB_ad4130_assertion wasDerivedFrom befree-20140225 NP409003.RAn56VcOe6TluIGd9BJC2ul7Ju_gxRogI-CL54RBB_ad4130_provenance.
- NP409003.RAn56VcOe6TluIGd9BJC2ul7Ju_gxRogI-CL54RBB_ad4130_assertion wasGeneratedBy ECO_0000203 NP409003.RAn56VcOe6TluIGd9BJC2ul7Ju_gxRogI-CL54RBB_ad4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP409003.RAn56VcOe6TluIGd9BJC2ul7Ju_gxRogI-CL54RBB_ad4130_provenance.