Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP892793.RAYHzdBZ5CN_M_-Bh8A7tBaInHGyhOoGv1T1mQ0yd0EMo130_assertion> ?p ?o ?g. }
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- NP892793.RAYHzdBZ5CN_M_-Bh8A7tBaInHGyhOoGv1T1mQ0yd0EMo130_assertion type Assertion NP892793.RAYHzdBZ5CN_M_-Bh8A7tBaInHGyhOoGv1T1mQ0yd0EMo130_head.
- NP892793.RAYHzdBZ5CN_M_-Bh8A7tBaInHGyhOoGv1T1mQ0yd0EMo130_assertion description "[The association of homozygous TT genotype with decreased CSF mononuclear leukocyte (ML) count not only suggests a clinical significance of this SNP, but indicates its potential to assist in the clinical assessment of suspected TBM, where delay is critical and diagnosis is difficult.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892793.RAYHzdBZ5CN_M_-Bh8A7tBaInHGyhOoGv1T1mQ0yd0EMo130_provenance.
- NP892793.RAYHzdBZ5CN_M_-Bh8A7tBaInHGyhOoGv1T1mQ0yd0EMo130_assertion evidence source_evidence_literature NP892793.RAYHzdBZ5CN_M_-Bh8A7tBaInHGyhOoGv1T1mQ0yd0EMo130_provenance.
- NP892793.RAYHzdBZ5CN_M_-Bh8A7tBaInHGyhOoGv1T1mQ0yd0EMo130_assertion SIO_000772 21556333 NP892793.RAYHzdBZ5CN_M_-Bh8A7tBaInHGyhOoGv1T1mQ0yd0EMo130_provenance.
- NP892793.RAYHzdBZ5CN_M_-Bh8A7tBaInHGyhOoGv1T1mQ0yd0EMo130_assertion wasDerivedFrom befree-2016 NP892793.RAYHzdBZ5CN_M_-Bh8A7tBaInHGyhOoGv1T1mQ0yd0EMo130_provenance.
- NP892793.RAYHzdBZ5CN_M_-Bh8A7tBaInHGyhOoGv1T1mQ0yd0EMo130_assertion wasGeneratedBy ECO_0000203 NP892793.RAYHzdBZ5CN_M_-Bh8A7tBaInHGyhOoGv1T1mQ0yd0EMo130_provenance.