Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP749868.RAwvDe8jGbYcqwcLtJviGlHpAoTXG2-R6-0Zn7GiTdtUU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP749868.RAwvDe8jGbYcqwcLtJviGlHpAoTXG2-R6-0Zn7GiTdtUU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP749868.RAwvDe8jGbYcqwcLtJviGlHpAoTXG2-R6-0Zn7GiTdtUU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP749868.RAwvDe8jGbYcqwcLtJviGlHpAoTXG2-R6-0Zn7GiTdtUU130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP749868.RAwvDe8jGbYcqwcLtJviGlHpAoTXG2-R6-0Zn7GiTdtUU130_provenance.