Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP1212.RA7EqwkhCxUvS9ql6GzhQP438aD0xdN0u2B6OMnHlukDk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP1212.RA7EqwkhCxUvS9ql6GzhQP438aD0xdN0u2B6OMnHlukDk130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1212.RA7EqwkhCxUvS9ql6GzhQP438aD0xdN0u2B6OMnHlukDk130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1212.RA7EqwkhCxUvS9ql6GzhQP438aD0xdN0u2B6OMnHlukDk130_provenance.
- NP1212.RA7EqwkhCxUvS9ql6GzhQP438aD0xdN0u2B6OMnHlukDk130_assertion description "[Mutations in eight genes (PPT1/CLN1, TPP1/CLN2, CLN3, CLN5, CLN6, MFSD8/CLN7, CLN8) have been identified and several more are predicted to exist, including two provisionally named CLN4 and CLN9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1212.RA7EqwkhCxUvS9ql6GzhQP438aD0xdN0u2B6OMnHlukDk130_provenance.
- NP1212.RA7EqwkhCxUvS9ql6GzhQP438aD0xdN0u2B6OMnHlukDk130_assertion evidence source_evidence_curated NP1212.RA7EqwkhCxUvS9ql6GzhQP438aD0xdN0u2B6OMnHlukDk130_provenance.
- NP1212.RA7EqwkhCxUvS9ql6GzhQP438aD0xdN0u2B6OMnHlukDk130_assertion SIO_000772 21990111 NP1212.RA7EqwkhCxUvS9ql6GzhQP438aD0xdN0u2B6OMnHlukDk130_provenance.
- NP1212.RA7EqwkhCxUvS9ql6GzhQP438aD0xdN0u2B6OMnHlukDk130_assertion wasDerivedFrom uniprot-20130724 NP1212.RA7EqwkhCxUvS9ql6GzhQP438aD0xdN0u2B6OMnHlukDk130_provenance.
- NP1212.RA7EqwkhCxUvS9ql6GzhQP438aD0xdN0u2B6OMnHlukDk130_assertion wasGeneratedBy ECO_0000218 NP1212.RA7EqwkhCxUvS9ql6GzhQP438aD0xdN0u2B6OMnHlukDk130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP1212.RA7EqwkhCxUvS9ql6GzhQP438aD0xdN0u2B6OMnHlukDk130_provenance.