Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP866976.RAEg0XFI_-Rwr1o4EpXiS8jQIQ2AfPBBDJ4f18faDqhBA130_assertion> ?p ?o ?g. }
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- NP866976.RAEg0XFI_-Rwr1o4EpXiS8jQIQ2AfPBBDJ4f18faDqhBA130_assertion type Assertion NP866976.RAEg0XFI_-Rwr1o4EpXiS8jQIQ2AfPBBDJ4f18faDqhBA130_head.
- NP866976.RAEg0XFI_-Rwr1o4EpXiS8jQIQ2AfPBBDJ4f18faDqhBA130_assertion description "[EEC syndrome type 3 with a heterozygous germline mutation in the P63 gene and B cell lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866976.RAEg0XFI_-Rwr1o4EpXiS8jQIQ2AfPBBDJ4f18faDqhBA130_provenance.
- NP866976.RAEg0XFI_-Rwr1o4EpXiS8jQIQ2AfPBBDJ4f18faDqhBA130_assertion evidence source_evidence_literature NP866976.RAEg0XFI_-Rwr1o4EpXiS8jQIQ2AfPBBDJ4f18faDqhBA130_provenance.
- NP866976.RAEg0XFI_-Rwr1o4EpXiS8jQIQ2AfPBBDJ4f18faDqhBA130_assertion SIO_000772 12838557 NP866976.RAEg0XFI_-Rwr1o4EpXiS8jQIQ2AfPBBDJ4f18faDqhBA130_provenance.
- NP866976.RAEg0XFI_-Rwr1o4EpXiS8jQIQ2AfPBBDJ4f18faDqhBA130_assertion wasDerivedFrom befree-20140225 NP866976.RAEg0XFI_-Rwr1o4EpXiS8jQIQ2AfPBBDJ4f18faDqhBA130_provenance.
- NP866976.RAEg0XFI_-Rwr1o4EpXiS8jQIQ2AfPBBDJ4f18faDqhBA130_assertion wasGeneratedBy ECO_0000203 NP866976.RAEg0XFI_-Rwr1o4EpXiS8jQIQ2AfPBBDJ4f18faDqhBA130_provenance.