Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP868223.RA2Eh5ZLfpC-TLBdWNqreQ3D_UVV6gJVAdmpT4srJFTRY130_assertion> ?p ?o ?g. }
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- NP868223.RA2Eh5ZLfpC-TLBdWNqreQ3D_UVV6gJVAdmpT4srJFTRY130_assertion type Assertion NP868223.RA2Eh5ZLfpC-TLBdWNqreQ3D_UVV6gJVAdmpT4srJFTRY130_head.
- NP868223.RA2Eh5ZLfpC-TLBdWNqreQ3D_UVV6gJVAdmpT4srJFTRY130_assertion description "[In the context of NPC, HLA genetic risk complete autosomal di-haplomic sequencing will enable testing of the Wee unitary origin hypothesis of NPC risk even among populations with no apparent mongoloid affinity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868223.RA2Eh5ZLfpC-TLBdWNqreQ3D_UVV6gJVAdmpT4srJFTRY130_provenance.
- NP868223.RA2Eh5ZLfpC-TLBdWNqreQ3D_UVV6gJVAdmpT4srJFTRY130_assertion evidence source_evidence_literature NP868223.RA2Eh5ZLfpC-TLBdWNqreQ3D_UVV6gJVAdmpT4srJFTRY130_provenance.
- NP868223.RA2Eh5ZLfpC-TLBdWNqreQ3D_UVV6gJVAdmpT4srJFTRY130_assertion SIO_000772 21272439 NP868223.RA2Eh5ZLfpC-TLBdWNqreQ3D_UVV6gJVAdmpT4srJFTRY130_provenance.
- NP868223.RA2Eh5ZLfpC-TLBdWNqreQ3D_UVV6gJVAdmpT4srJFTRY130_assertion wasDerivedFrom befree-2016 NP868223.RA2Eh5ZLfpC-TLBdWNqreQ3D_UVV6gJVAdmpT4srJFTRY130_provenance.
- NP868223.RA2Eh5ZLfpC-TLBdWNqreQ3D_UVV6gJVAdmpT4srJFTRY130_assertion wasGeneratedBy ECO_0000203 NP868223.RA2Eh5ZLfpC-TLBdWNqreQ3D_UVV6gJVAdmpT4srJFTRY130_provenance.