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- source_evidence_literature type ECO_0000212 NP856088.RAPeyOpdX_k5F6ZQ7b4tYIs9VR13iRt2ebhZSJueugPk4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP856088.RAPeyOpdX_k5F6ZQ7b4tYIs9VR13iRt2ebhZSJueugPk4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP856088.RAPeyOpdX_k5F6ZQ7b4tYIs9VR13iRt2ebhZSJueugPk4130_provenance.
- NP856088.RAPeyOpdX_k5F6ZQ7b4tYIs9VR13iRt2ebhZSJueugPk4130_assertion description "[ICF should be suspected in children with facial dysmorphism who present with recurrent infections especially in highly inbred populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856088.RAPeyOpdX_k5F6ZQ7b4tYIs9VR13iRt2ebhZSJueugPk4130_provenance.
- NP856088.RAPeyOpdX_k5F6ZQ7b4tYIs9VR13iRt2ebhZSJueugPk4130_assertion evidence source_evidence_literature NP856088.RAPeyOpdX_k5F6ZQ7b4tYIs9VR13iRt2ebhZSJueugPk4130_provenance.
- NP856088.RAPeyOpdX_k5F6ZQ7b4tYIs9VR13iRt2ebhZSJueugPk4130_assertion SIO_000772 21120685 NP856088.RAPeyOpdX_k5F6ZQ7b4tYIs9VR13iRt2ebhZSJueugPk4130_provenance.
- NP856088.RAPeyOpdX_k5F6ZQ7b4tYIs9VR13iRt2ebhZSJueugPk4130_assertion wasDerivedFrom befree-2016 NP856088.RAPeyOpdX_k5F6ZQ7b4tYIs9VR13iRt2ebhZSJueugPk4130_provenance.
- NP856088.RAPeyOpdX_k5F6ZQ7b4tYIs9VR13iRt2ebhZSJueugPk4130_assertion wasGeneratedBy ECO_0000203 NP856088.RAPeyOpdX_k5F6ZQ7b4tYIs9VR13iRt2ebhZSJueugPk4130_provenance.
- befree-2016 importedOn "2016-02-19" NP856088.RAPeyOpdX_k5F6ZQ7b4tYIs9VR13iRt2ebhZSJueugPk4130_provenance.