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- NP204778.RAH2nz244T_VT5KutNiBe1RptemCAY0D8VKSKNsfb2avY130_assertion type Assertion NP204778.RAH2nz244T_VT5KutNiBe1RptemCAY0D8VKSKNsfb2avY130_head.
- NP204778.RAH2nz244T_VT5KutNiBe1RptemCAY0D8VKSKNsfb2avY130_assertion description "[identification of six novel point mutations and one large intragenic deletion in hereditary spastic paraplegia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP204778.RAH2nz244T_VT5KutNiBe1RptemCAY0D8VKSKNsfb2avY130_provenance.
- NP204778.RAH2nz244T_VT5KutNiBe1RptemCAY0D8VKSKNsfb2avY130_assertion evidence source_evidence_literature NP204778.RAH2nz244T_VT5KutNiBe1RptemCAY0D8VKSKNsfb2avY130_provenance.
- NP204778.RAH2nz244T_VT5KutNiBe1RptemCAY0D8VKSKNsfb2avY130_assertion SIO_000772 18200586 NP204778.RAH2nz244T_VT5KutNiBe1RptemCAY0D8VKSKNsfb2avY130_provenance.
- NP204778.RAH2nz244T_VT5KutNiBe1RptemCAY0D8VKSKNsfb2avY130_assertion wasDerivedFrom lhgdn-20090331 NP204778.RAH2nz244T_VT5KutNiBe1RptemCAY0D8VKSKNsfb2avY130_provenance.
- NP204778.RAH2nz244T_VT5KutNiBe1RptemCAY0D8VKSKNsfb2avY130_assertion wasGeneratedBy ECO_0000203 NP204778.RAH2nz244T_VT5KutNiBe1RptemCAY0D8VKSKNsfb2avY130_provenance.