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- NP788020.RA8pynrhWPF9gQwJuaw8KlDrsCeqAEfoxu8igmzcxtauw130_assertion type Assertion NP788020.RA8pynrhWPF9gQwJuaw8KlDrsCeqAEfoxu8igmzcxtauw130_head.
- NP788020.RA8pynrhWPF9gQwJuaw8KlDrsCeqAEfoxu8igmzcxtauw130_assertion wasGeneratedBy ECO_0000203 NP788020.RA8pynrhWPF9gQwJuaw8KlDrsCeqAEfoxu8igmzcxtauw130_provenance.
- NP788020.RA8pynrhWPF9gQwJuaw8KlDrsCeqAEfoxu8igmzcxtauw130_assertion wasDerivedFrom befree-2016 NP788020.RA8pynrhWPF9gQwJuaw8KlDrsCeqAEfoxu8igmzcxtauw130_provenance.
- NP788020.RA8pynrhWPF9gQwJuaw8KlDrsCeqAEfoxu8igmzcxtauw130_assertion SIO_000772 20083694 NP788020.RA8pynrhWPF9gQwJuaw8KlDrsCeqAEfoxu8igmzcxtauw130_provenance.
- NP788020.RA8pynrhWPF9gQwJuaw8KlDrsCeqAEfoxu8igmzcxtauw130_assertion evidence source_evidence_literature NP788020.RA8pynrhWPF9gQwJuaw8KlDrsCeqAEfoxu8igmzcxtauw130_provenance.
- NP788020.RA8pynrhWPF9gQwJuaw8KlDrsCeqAEfoxu8igmzcxtauw130_assertion description "[Absence of LEMD3 mutation in the exons and splice sites of a family with BOS suggests that there is genetic heterogeneity for this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788020.RA8pynrhWPF9gQwJuaw8KlDrsCeqAEfoxu8igmzcxtauw130_provenance.