Matches in Nanopublications for { ?s ?p "[The most common form of HSP is caused by mutations of the spastin gene (SPAST), located on chromosome 2p21-p22, which encodes spastin, one of the ATPases associated with diverse cellular activities (AAA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP759507.RAgcdYlEsf3tTfvr_3_c-kgmkr_V7euz5H_oYHkwiEXXU130_assertion description "[The most common form of HSP is caused by mutations of the spastin gene (SPAST), located on chromosome 2p21-p22, which encodes spastin, one of the ATPases associated with diverse cellular activities (AAA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP759507.RAgcdYlEsf3tTfvr_3_c-kgmkr_V7euz5H_oYHkwiEXXU130_provenance.
- NP879913.RAntNRwpb6VDkBVCT1gw5J-iEkdLvzf_oxbyZcosRtI8E130_assertion description "[The most common form of HSP is caused by mutations of the spastin gene (SPAST), located on chromosome 2p21-p22, which encodes spastin, one of the ATPases associated with diverse cellular activities (AAA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP879913.RAntNRwpb6VDkBVCT1gw5J-iEkdLvzf_oxbyZcosRtI8E130_provenance.
- NP513777.RA3CNwd-gPKw8GuNz_BHWaM8z4tbfBNoIPh34eOyizxyo130_assertion description "[The most common form of HSP is caused by mutations of the spastin gene (SPAST), located on chromosome 2p21-p22, which encodes spastin, one of the ATPases associated with diverse cellular activities (AAA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP513777.RA3CNwd-gPKw8GuNz_BHWaM8z4tbfBNoIPh34eOyizxyo130_provenance.