Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3204.RAaXQ2m4Qoh-NzgVUB4MuN6TqERw6cMMSsIdgTeVWdSIo130_assertion> ?p ?o ?g. }
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- NP3204.RAaXQ2m4Qoh-NzgVUB4MuN6TqERw6cMMSsIdgTeVWdSIo130_assertion type Assertion NP3204.RAaXQ2m4Qoh-NzgVUB4MuN6TqERw6cMMSsIdgTeVWdSIo130_head.
- NP3204.RAaXQ2m4Qoh-NzgVUB4MuN6TqERw6cMMSsIdgTeVWdSIo130_assertion description "[Because not all of our patients harbored mutations in IFT122, CED seems to be genetically heterogeneous.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3204.RAaXQ2m4Qoh-NzgVUB4MuN6TqERw6cMMSsIdgTeVWdSIo130_provenance.
- NP3204.RAaXQ2m4Qoh-NzgVUB4MuN6TqERw6cMMSsIdgTeVWdSIo130_assertion evidence source_evidence_curated NP3204.RAaXQ2m4Qoh-NzgVUB4MuN6TqERw6cMMSsIdgTeVWdSIo130_provenance.
- NP3204.RAaXQ2m4Qoh-NzgVUB4MuN6TqERw6cMMSsIdgTeVWdSIo130_assertion SIO_000772 20493458 NP3204.RAaXQ2m4Qoh-NzgVUB4MuN6TqERw6cMMSsIdgTeVWdSIo130_provenance.
- NP3204.RAaXQ2m4Qoh-NzgVUB4MuN6TqERw6cMMSsIdgTeVWdSIo130_assertion wasDerivedFrom uniprot-20130724 NP3204.RAaXQ2m4Qoh-NzgVUB4MuN6TqERw6cMMSsIdgTeVWdSIo130_provenance.
- NP3204.RAaXQ2m4Qoh-NzgVUB4MuN6TqERw6cMMSsIdgTeVWdSIo130_assertion wasGeneratedBy ECO_0000218 NP3204.RAaXQ2m4Qoh-NzgVUB4MuN6TqERw6cMMSsIdgTeVWdSIo130_provenance.