Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1963.RAgTsg5qcE2yxpaJT7fUFY6b_hPFCm_iQ189NZWaF5rlI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1963.RAgTsg5qcE2yxpaJT7fUFY6b_hPFCm_iQ189NZWaF5rlI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1963.RAgTsg5qcE2yxpaJT7fUFY6b_hPFCm_iQ189NZWaF5rlI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1963.RAgTsg5qcE2yxpaJT7fUFY6b_hPFCm_iQ189NZWaF5rlI130_provenance.
- NP1963.RAgTsg5qcE2yxpaJT7fUFY6b_hPFCm_iQ189NZWaF5rlI130_assertion description "[Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1963.RAgTsg5qcE2yxpaJT7fUFY6b_hPFCm_iQ189NZWaF5rlI130_provenance.
- NP1963.RAgTsg5qcE2yxpaJT7fUFY6b_hPFCm_iQ189NZWaF5rlI130_assertion evidence source_evidence_curated NP1963.RAgTsg5qcE2yxpaJT7fUFY6b_hPFCm_iQ189NZWaF5rlI130_provenance.
- NP1963.RAgTsg5qcE2yxpaJT7fUFY6b_hPFCm_iQ189NZWaF5rlI130_assertion SIO_000772 23455423 NP1963.RAgTsg5qcE2yxpaJT7fUFY6b_hPFCm_iQ189NZWaF5rlI130_provenance.
- NP1963.RAgTsg5qcE2yxpaJT7fUFY6b_hPFCm_iQ189NZWaF5rlI130_assertion wasDerivedFrom uniprot-20150221 NP1963.RAgTsg5qcE2yxpaJT7fUFY6b_hPFCm_iQ189NZWaF5rlI130_provenance.
- NP1963.RAgTsg5qcE2yxpaJT7fUFY6b_hPFCm_iQ189NZWaF5rlI130_assertion wasGeneratedBy ECO_0000218 NP1963.RAgTsg5qcE2yxpaJT7fUFY6b_hPFCm_iQ189NZWaF5rlI130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP1963.RAgTsg5qcE2yxpaJT7fUFY6b_hPFCm_iQ189NZWaF5rlI130_provenance.