Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7872.RASPUPeNuPcJps7zl7X6Ifueiw5qnWFacQ14PaGadT2yc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP7872.RASPUPeNuPcJps7zl7X6Ifueiw5qnWFacQ14PaGadT2yc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7872.RASPUPeNuPcJps7zl7X6Ifueiw5qnWFacQ14PaGadT2yc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7872.RASPUPeNuPcJps7zl7X6Ifueiw5qnWFacQ14PaGadT2yc130_provenance.
- NP7872.RASPUPeNuPcJps7zl7X6Ifueiw5qnWFacQ14PaGadT2yc130_assertion description "[De novo mutations in HCN1 cause early infantile epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7872.RASPUPeNuPcJps7zl7X6Ifueiw5qnWFacQ14PaGadT2yc130_provenance.
- NP7872.RASPUPeNuPcJps7zl7X6Ifueiw5qnWFacQ14PaGadT2yc130_assertion evidence source_evidence_curated NP7872.RASPUPeNuPcJps7zl7X6Ifueiw5qnWFacQ14PaGadT2yc130_provenance.
- NP7872.RASPUPeNuPcJps7zl7X6Ifueiw5qnWFacQ14PaGadT2yc130_assertion SIO_000772 24747641 NP7872.RASPUPeNuPcJps7zl7X6Ifueiw5qnWFacQ14PaGadT2yc130_provenance.
- NP7872.RASPUPeNuPcJps7zl7X6Ifueiw5qnWFacQ14PaGadT2yc130_assertion wasDerivedFrom uniprot-2016 NP7872.RASPUPeNuPcJps7zl7X6Ifueiw5qnWFacQ14PaGadT2yc130_provenance.
- NP7872.RASPUPeNuPcJps7zl7X6Ifueiw5qnWFacQ14PaGadT2yc130_assertion wasGeneratedBy ECO_0000218 NP7872.RASPUPeNuPcJps7zl7X6Ifueiw5qnWFacQ14PaGadT2yc130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7872.RASPUPeNuPcJps7zl7X6Ifueiw5qnWFacQ14PaGadT2yc130_provenance.