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- NP486909.RATgopwc0OD-tNI6IV3Qd4_slkmWHfMjQ-eojK_r3ZsHE130_assertion type Assertion NP486909.RATgopwc0OD-tNI6IV3Qd4_slkmWHfMjQ-eojK_r3ZsHE130_head.
- NP486909.RATgopwc0OD-tNI6IV3Qd4_slkmWHfMjQ-eojK_r3ZsHE130_assertion wasGeneratedBy ECO_0000203 NP486909.RATgopwc0OD-tNI6IV3Qd4_slkmWHfMjQ-eojK_r3ZsHE130_provenance.
- NP486909.RATgopwc0OD-tNI6IV3Qd4_slkmWHfMjQ-eojK_r3ZsHE130_assertion wasDerivedFrom befree-20150227 NP486909.RATgopwc0OD-tNI6IV3Qd4_slkmWHfMjQ-eojK_r3ZsHE130_provenance.
- NP486909.RATgopwc0OD-tNI6IV3Qd4_slkmWHfMjQ-eojK_r3ZsHE130_assertion SIO_000772 22965130 NP486909.RATgopwc0OD-tNI6IV3Qd4_slkmWHfMjQ-eojK_r3ZsHE130_provenance.
- NP486909.RATgopwc0OD-tNI6IV3Qd4_slkmWHfMjQ-eojK_r3ZsHE130_assertion evidence source_evidence_literature NP486909.RATgopwc0OD-tNI6IV3Qd4_slkmWHfMjQ-eojK_r3ZsHE130_provenance.
- NP486909.RATgopwc0OD-tNI6IV3Qd4_slkmWHfMjQ-eojK_r3ZsHE130_assertion description "[Mutations in immunoglobulin µ-binding protein 2 (Ighmbp2) cause distal spinal muscular atrophy type 1 (DSMA1), an autosomal recessive disease that is clinically characterized by distal limb weakness and respiratory distress.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP486909.RATgopwc0OD-tNI6IV3Qd4_slkmWHfMjQ-eojK_r3ZsHE130_provenance.