Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_assertion> ?p ?o ?g. }
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- NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_assertion type Assertion NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_head.
- NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_assertion description "[Mutations in the DNM2 gene cause two hereditary neuromuscular disorders: dominant centronuclear myopathy and Charcot-Marie-Tooth peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_provenance.
- NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_assertion evidence source_evidence_literature NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_provenance.
- NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_assertion SIO_000772 23609221 NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_provenance.
- NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_assertion wasDerivedFrom befree-20150227 NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_provenance.
- NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_assertion wasGeneratedBy ECO_0000203 NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_provenance.