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- source_evidence_literature type ECO_0000212 NP831595.RAVMC6j8PD-AKGHNsPy0uxvGF76s924_FMLT_uROp3lbU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP831595.RAVMC6j8PD-AKGHNsPy0uxvGF76s924_FMLT_uROp3lbU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP831595.RAVMC6j8PD-AKGHNsPy0uxvGF76s924_FMLT_uROp3lbU130_provenance.
- NP831595.RAVMC6j8PD-AKGHNsPy0uxvGF76s924_FMLT_uROp3lbU130_assertion description "[The novel findings included a set of genes (DCDC2, DYX1C1, KIAA0319) related to a neurological disease dyslexia suggesting their potential involvement in ciliary functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831595.RAVMC6j8PD-AKGHNsPy0uxvGF76s924_FMLT_uROp3lbU130_provenance.
- NP831595.RAVMC6j8PD-AKGHNsPy0uxvGF76s924_FMLT_uROp3lbU130_assertion evidence source_evidence_literature NP831595.RAVMC6j8PD-AKGHNsPy0uxvGF76s924_FMLT_uROp3lbU130_provenance.
- NP831595.RAVMC6j8PD-AKGHNsPy0uxvGF76s924_FMLT_uROp3lbU130_assertion SIO_000772 22558177 NP831595.RAVMC6j8PD-AKGHNsPy0uxvGF76s924_FMLT_uROp3lbU130_provenance.
- NP831595.RAVMC6j8PD-AKGHNsPy0uxvGF76s924_FMLT_uROp3lbU130_assertion wasDerivedFrom befree-20150227 NP831595.RAVMC6j8PD-AKGHNsPy0uxvGF76s924_FMLT_uROp3lbU130_provenance.
- NP831595.RAVMC6j8PD-AKGHNsPy0uxvGF76s924_FMLT_uROp3lbU130_assertion wasGeneratedBy ECO_0000203 NP831595.RAVMC6j8PD-AKGHNsPy0uxvGF76s924_FMLT_uROp3lbU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP831595.RAVMC6j8PD-AKGHNsPy0uxvGF76s924_FMLT_uROp3lbU130_provenance.