Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP709995.RAuUNag7ZDnmwQ4pBU_bYwL9uB4sn-rRZ00bpNRAsc_LE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP709995.RAuUNag7ZDnmwQ4pBU_bYwL9uB4sn-rRZ00bpNRAsc_LE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP709995.RAuUNag7ZDnmwQ4pBU_bYwL9uB4sn-rRZ00bpNRAsc_LE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP709995.RAuUNag7ZDnmwQ4pBU_bYwL9uB4sn-rRZ00bpNRAsc_LE130_provenance.
- NP709995.RAuUNag7ZDnmwQ4pBU_bYwL9uB4sn-rRZ00bpNRAsc_LE130_assertion description "[We conclude that this kindred demonstrates a considerable overlap between cerebellar ataxia and spastic paraplegia, emphasizing the marked clinical heterogeneity of HSP associated with spastin mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709995.RAuUNag7ZDnmwQ4pBU_bYwL9uB4sn-rRZ00bpNRAsc_LE130_provenance.
- NP709995.RAuUNag7ZDnmwQ4pBU_bYwL9uB4sn-rRZ00bpNRAsc_LE130_assertion evidence source_evidence_literature NP709995.RAuUNag7ZDnmwQ4pBU_bYwL9uB4sn-rRZ00bpNRAsc_LE130_provenance.
- NP709995.RAuUNag7ZDnmwQ4pBU_bYwL9uB4sn-rRZ00bpNRAsc_LE130_assertion SIO_000772 15667412 NP709995.RAuUNag7ZDnmwQ4pBU_bYwL9uB4sn-rRZ00bpNRAsc_LE130_provenance.
- NP709995.RAuUNag7ZDnmwQ4pBU_bYwL9uB4sn-rRZ00bpNRAsc_LE130_assertion wasDerivedFrom befree-20150227 NP709995.RAuUNag7ZDnmwQ4pBU_bYwL9uB4sn-rRZ00bpNRAsc_LE130_provenance.
- NP709995.RAuUNag7ZDnmwQ4pBU_bYwL9uB4sn-rRZ00bpNRAsc_LE130_assertion wasGeneratedBy ECO_0000203 NP709995.RAuUNag7ZDnmwQ4pBU_bYwL9uB4sn-rRZ00bpNRAsc_LE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP709995.RAuUNag7ZDnmwQ4pBU_bYwL9uB4sn-rRZ00bpNRAsc_LE130_provenance.