Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP648108.RAEOL-YmfCsO3rYPhTdoJfRLtc-mXgTUKWnLaC-eTgnsE130_assertion> ?p ?o ?g. }
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- NP648108.RAEOL-YmfCsO3rYPhTdoJfRLtc-mXgTUKWnLaC-eTgnsE130_assertion type Assertion NP648108.RAEOL-YmfCsO3rYPhTdoJfRLtc-mXgTUKWnLaC-eTgnsE130_head.
- NP648108.RAEOL-YmfCsO3rYPhTdoJfRLtc-mXgTUKWnLaC-eTgnsE130_assertion description "[A total of eight loci for autosomal dominant hereditary spastic paraplegia (ADHSP) has been mapped to chromosome 14q, 2p, 15q, 8q, 10q, 12q, 19q, 2q, respectively, among which the SPG4 gene on chromosome 2p21-22 encoding spastin, an ATPase of the AAA family, accounts for 40-50% of all ADHSP families and is expressed in both adult and fetal tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648108.RAEOL-YmfCsO3rYPhTdoJfRLtc-mXgTUKWnLaC-eTgnsE130_provenance.
- NP648108.RAEOL-YmfCsO3rYPhTdoJfRLtc-mXgTUKWnLaC-eTgnsE130_assertion evidence source_evidence_literature NP648108.RAEOL-YmfCsO3rYPhTdoJfRLtc-mXgTUKWnLaC-eTgnsE130_provenance.
- NP648108.RAEOL-YmfCsO3rYPhTdoJfRLtc-mXgTUKWnLaC-eTgnsE130_assertion SIO_000772 12736085 NP648108.RAEOL-YmfCsO3rYPhTdoJfRLtc-mXgTUKWnLaC-eTgnsE130_provenance.
- NP648108.RAEOL-YmfCsO3rYPhTdoJfRLtc-mXgTUKWnLaC-eTgnsE130_assertion wasDerivedFrom befree-20140225 NP648108.RAEOL-YmfCsO3rYPhTdoJfRLtc-mXgTUKWnLaC-eTgnsE130_provenance.
- NP648108.RAEOL-YmfCsO3rYPhTdoJfRLtc-mXgTUKWnLaC-eTgnsE130_assertion wasGeneratedBy ECO_0000203 NP648108.RAEOL-YmfCsO3rYPhTdoJfRLtc-mXgTUKWnLaC-eTgnsE130_provenance.