Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP9415.RAd_0uPhCpIwKf-g86frNc2C5T6wkgTNp_X4XicUqp3Qs130_assertion> ?p ?o ?g. }
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- NP9415.RAd_0uPhCpIwKf-g86frNc2C5T6wkgTNp_X4XicUqp3Qs130_assertion type Assertion NP9415.RAd_0uPhCpIwKf-g86frNc2C5T6wkgTNp_X4XicUqp3Qs130_head.
- NP9415.RAd_0uPhCpIwKf-g86frNc2C5T6wkgTNp_X4XicUqp3Qs130_assertion description "[Spectrum of mutations in the OCRL1 gene in the Lowe oculocerebrorenal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9415.RAd_0uPhCpIwKf-g86frNc2C5T6wkgTNp_X4XicUqp3Qs130_provenance.
- NP9415.RAd_0uPhCpIwKf-g86frNc2C5T6wkgTNp_X4XicUqp3Qs130_assertion evidence source_evidence_curated NP9415.RAd_0uPhCpIwKf-g86frNc2C5T6wkgTNp_X4XicUqp3Qs130_provenance.
- NP9415.RAd_0uPhCpIwKf-g86frNc2C5T6wkgTNp_X4XicUqp3Qs130_assertion SIO_000772 9199559 NP9415.RAd_0uPhCpIwKf-g86frNc2C5T6wkgTNp_X4XicUqp3Qs130_provenance.
- NP9415.RAd_0uPhCpIwKf-g86frNc2C5T6wkgTNp_X4XicUqp3Qs130_assertion wasDerivedFrom uniprot-2016 NP9415.RAd_0uPhCpIwKf-g86frNc2C5T6wkgTNp_X4XicUqp3Qs130_provenance.
- NP9415.RAd_0uPhCpIwKf-g86frNc2C5T6wkgTNp_X4XicUqp3Qs130_assertion wasGeneratedBy ECO_0000218 NP9415.RAd_0uPhCpIwKf-g86frNc2C5T6wkgTNp_X4XicUqp3Qs130_provenance.