Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1248402.RAv1S22BSGtGCWNq2C0k7_fxy3sZRBpFtAuzDN-wmNF44130_assertion> ?p ?o ?g. }
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- NP1248402.RAv1S22BSGtGCWNq2C0k7_fxy3sZRBpFtAuzDN-wmNF44130_assertion type Assertion NP1248402.RAv1S22BSGtGCWNq2C0k7_fxy3sZRBpFtAuzDN-wmNF44130_head.
- NP1248402.RAv1S22BSGtGCWNq2C0k7_fxy3sZRBpFtAuzDN-wmNF44130_assertion description "[Our findings broaden the genetic heterogeneity and refine the clinical spectrum of DYNC1H1, and have implications for molecular diagnostics of motor neuron diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1248402.RAv1S22BSGtGCWNq2C0k7_fxy3sZRBpFtAuzDN-wmNF44130_provenance.
- NP1248402.RAv1S22BSGtGCWNq2C0k7_fxy3sZRBpFtAuzDN-wmNF44130_assertion evidence source_evidence_literature NP1248402.RAv1S22BSGtGCWNq2C0k7_fxy3sZRBpFtAuzDN-wmNF44130_provenance.
- NP1248402.RAv1S22BSGtGCWNq2C0k7_fxy3sZRBpFtAuzDN-wmNF44130_assertion SIO_000772 25512093 NP1248402.RAv1S22BSGtGCWNq2C0k7_fxy3sZRBpFtAuzDN-wmNF44130_provenance.
- NP1248402.RAv1S22BSGtGCWNq2C0k7_fxy3sZRBpFtAuzDN-wmNF44130_assertion wasDerivedFrom befree-2016 NP1248402.RAv1S22BSGtGCWNq2C0k7_fxy3sZRBpFtAuzDN-wmNF44130_provenance.
- NP1248402.RAv1S22BSGtGCWNq2C0k7_fxy3sZRBpFtAuzDN-wmNF44130_assertion wasGeneratedBy ECO_0000203 NP1248402.RAv1S22BSGtGCWNq2C0k7_fxy3sZRBpFtAuzDN-wmNF44130_provenance.