Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP204778.RAH2nz244T_VT5KutNiBe1RptemCAY0D8VKSKNsfb2avY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP204778.RAH2nz244T_VT5KutNiBe1RptemCAY0D8VKSKNsfb2avY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP204778.RAH2nz244T_VT5KutNiBe1RptemCAY0D8VKSKNsfb2avY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP204778.RAH2nz244T_VT5KutNiBe1RptemCAY0D8VKSKNsfb2avY130_provenance.
- 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.
- lhgdn-20090331 importedOn "2009-03-31" NP204778.RAH2nz244T_VT5KutNiBe1RptemCAY0D8VKSKNsfb2avY130_provenance.