Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP749868.RAwvDe8jGbYcqwcLtJviGlHpAoTXG2-R6-0Zn7GiTdtUU130_assertion> ?p ?o ?g. }
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- NP749868.RAwvDe8jGbYcqwcLtJviGlHpAoTXG2-R6-0Zn7GiTdtUU130_assertion type Assertion NP749868.RAwvDe8jGbYcqwcLtJviGlHpAoTXG2-R6-0Zn7GiTdtUU130_head.
- NP749868.RAwvDe8jGbYcqwcLtJviGlHpAoTXG2-R6-0Zn7GiTdtUU130_assertion description "[Mice with heterozygous deletion of exon 2 in Reep1 displayed a gait disorder closely resembling SPG31 in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749868.RAwvDe8jGbYcqwcLtJviGlHpAoTXG2-R6-0Zn7GiTdtUU130_provenance.
- NP749868.RAwvDe8jGbYcqwcLtJviGlHpAoTXG2-R6-0Zn7GiTdtUU130_assertion evidence source_evidence_literature NP749868.RAwvDe8jGbYcqwcLtJviGlHpAoTXG2-R6-0Zn7GiTdtUU130_provenance.
- NP749868.RAwvDe8jGbYcqwcLtJviGlHpAoTXG2-R6-0Zn7GiTdtUU130_assertion SIO_000772 24051375 NP749868.RAwvDe8jGbYcqwcLtJviGlHpAoTXG2-R6-0Zn7GiTdtUU130_provenance.
- NP749868.RAwvDe8jGbYcqwcLtJviGlHpAoTXG2-R6-0Zn7GiTdtUU130_assertion wasDerivedFrom befree-20140225 NP749868.RAwvDe8jGbYcqwcLtJviGlHpAoTXG2-R6-0Zn7GiTdtUU130_provenance.
- NP749868.RAwvDe8jGbYcqwcLtJviGlHpAoTXG2-R6-0Zn7GiTdtUU130_assertion wasGeneratedBy ECO_0000203 NP749868.RAwvDe8jGbYcqwcLtJviGlHpAoTXG2-R6-0Zn7GiTdtUU130_provenance.