Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP710192.RAXMzP0jvIBoEjf2XeraRdrHWJ2qpf-Qydpkf5ni7u7Vs130_assertion> ?p ?o ?g. }
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- NP710192.RAXMzP0jvIBoEjf2XeraRdrHWJ2qpf-Qydpkf5ni7u7Vs130_assertion type Assertion NP710192.RAXMzP0jvIBoEjf2XeraRdrHWJ2qpf-Qydpkf5ni7u7Vs130_head.
- NP710192.RAXMzP0jvIBoEjf2XeraRdrHWJ2qpf-Qydpkf5ni7u7Vs130_assertion description "[Mutations in the SPG7 gene, which encodes paraplegin, are responsible for an autosomal recessive hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710192.RAXMzP0jvIBoEjf2XeraRdrHWJ2qpf-Qydpkf5ni7u7Vs130_provenance.
- NP710192.RAXMzP0jvIBoEjf2XeraRdrHWJ2qpf-Qydpkf5ni7u7Vs130_assertion evidence source_evidence_literature NP710192.RAXMzP0jvIBoEjf2XeraRdrHWJ2qpf-Qydpkf5ni7u7Vs130_provenance.
- NP710192.RAXMzP0jvIBoEjf2XeraRdrHWJ2qpf-Qydpkf5ni7u7Vs130_assertion SIO_000772 16534102 NP710192.RAXMzP0jvIBoEjf2XeraRdrHWJ2qpf-Qydpkf5ni7u7Vs130_provenance.
- NP710192.RAXMzP0jvIBoEjf2XeraRdrHWJ2qpf-Qydpkf5ni7u7Vs130_assertion wasDerivedFrom befree-20150227 NP710192.RAXMzP0jvIBoEjf2XeraRdrHWJ2qpf-Qydpkf5ni7u7Vs130_provenance.
- NP710192.RAXMzP0jvIBoEjf2XeraRdrHWJ2qpf-Qydpkf5ni7u7Vs130_assertion wasGeneratedBy ECO_0000203 NP710192.RAXMzP0jvIBoEjf2XeraRdrHWJ2qpf-Qydpkf5ni7u7Vs130_provenance.