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- source_evidence_literature type ECO_0000212 NP710192.RAXMzP0jvIBoEjf2XeraRdrHWJ2qpf-Qydpkf5ni7u7Vs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710192.RAXMzP0jvIBoEjf2XeraRdrHWJ2qpf-Qydpkf5ni7u7Vs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710192.RAXMzP0jvIBoEjf2XeraRdrHWJ2qpf-Qydpkf5ni7u7Vs130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP710192.RAXMzP0jvIBoEjf2XeraRdrHWJ2qpf-Qydpkf5ni7u7Vs130_provenance.