Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP708019.RAszevyhyG2CC0omJYA0RBKVOCaURnrS_sG9H3G_EWaoo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP708019.RAszevyhyG2CC0omJYA0RBKVOCaURnrS_sG9H3G_EWaoo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP708019.RAszevyhyG2CC0omJYA0RBKVOCaURnrS_sG9H3G_EWaoo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP708019.RAszevyhyG2CC0omJYA0RBKVOCaURnrS_sG9H3G_EWaoo130_provenance.
- NP708019.RAszevyhyG2CC0omJYA0RBKVOCaURnrS_sG9H3G_EWaoo130_assertion description "[Eighty-six M-D index patients from the Dutch national referral centre for M-D underwent neurological examination and were classified according to previously published criteria into definite, probable and possible M-D. Sequence analysis of the SGCE gene and screening for copy number variations were performed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708019.RAszevyhyG2CC0omJYA0RBKVOCaURnrS_sG9H3G_EWaoo130_provenance.
- NP708019.RAszevyhyG2CC0omJYA0RBKVOCaURnrS_sG9H3G_EWaoo130_assertion evidence source_evidence_literature NP708019.RAszevyhyG2CC0omJYA0RBKVOCaURnrS_sG9H3G_EWaoo130_provenance.
- NP708019.RAszevyhyG2CC0omJYA0RBKVOCaURnrS_sG9H3G_EWaoo130_assertion SIO_000772 19066193 NP708019.RAszevyhyG2CC0omJYA0RBKVOCaURnrS_sG9H3G_EWaoo130_provenance.
- NP708019.RAszevyhyG2CC0omJYA0RBKVOCaURnrS_sG9H3G_EWaoo130_assertion wasDerivedFrom befree-2016 NP708019.RAszevyhyG2CC0omJYA0RBKVOCaURnrS_sG9H3G_EWaoo130_provenance.
- NP708019.RAszevyhyG2CC0omJYA0RBKVOCaURnrS_sG9H3G_EWaoo130_assertion wasGeneratedBy ECO_0000203 NP708019.RAszevyhyG2CC0omJYA0RBKVOCaURnrS_sG9H3G_EWaoo130_provenance.
- befree-2016 importedOn "2016-02-19" NP708019.RAszevyhyG2CC0omJYA0RBKVOCaURnrS_sG9H3G_EWaoo130_provenance.