Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP917081.RAhnTiakAF2i0AjTYJGyuH2PcNgw302OfUcKMmAMvA7Hk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP917081.RAhnTiakAF2i0AjTYJGyuH2PcNgw302OfUcKMmAMvA7Hk130_assertion type Assertion NP917081.RAhnTiakAF2i0AjTYJGyuH2PcNgw302OfUcKMmAMvA7Hk130_head.
- NP917081.RAhnTiakAF2i0AjTYJGyuH2PcNgw302OfUcKMmAMvA7Hk130_assertion description "[Mutations in both alleles of the tumour suppressor gene coding for merlin/schwannomin, an ERM family protein, cause the hereditary disease neurofibromatosis type 2 (NF2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917081.RAhnTiakAF2i0AjTYJGyuH2PcNgw302OfUcKMmAMvA7Hk130_provenance.
- NP917081.RAhnTiakAF2i0AjTYJGyuH2PcNgw302OfUcKMmAMvA7Hk130_assertion evidence source_evidence_literature NP917081.RAhnTiakAF2i0AjTYJGyuH2PcNgw302OfUcKMmAMvA7Hk130_provenance.
- NP917081.RAhnTiakAF2i0AjTYJGyuH2PcNgw302OfUcKMmAMvA7Hk130_assertion SIO_000772 11773000 NP917081.RAhnTiakAF2i0AjTYJGyuH2PcNgw302OfUcKMmAMvA7Hk130_provenance.
- NP917081.RAhnTiakAF2i0AjTYJGyuH2PcNgw302OfUcKMmAMvA7Hk130_assertion wasDerivedFrom befree-20140225 NP917081.RAhnTiakAF2i0AjTYJGyuH2PcNgw302OfUcKMmAMvA7Hk130_provenance.
- NP917081.RAhnTiakAF2i0AjTYJGyuH2PcNgw302OfUcKMmAMvA7Hk130_assertion wasGeneratedBy ECO_0000203 NP917081.RAhnTiakAF2i0AjTYJGyuH2PcNgw302OfUcKMmAMvA7Hk130_provenance.