Matches in Nanopublications for { ?s ?p "[A mechanism for its pathogenesis has not been identified, but loss of function of EXT genes is implicated in sporadic and hereditary multiple osteochondromas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP265027.RAwvCjhcwYMJmtMHTt75ixwMs9QqBK281Wy9zeRGVIjRA130_assertion description "[A mechanism for its pathogenesis has not been identified, but loss of function of EXT genes is implicated in sporadic and hereditary multiple osteochondromas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265027.RAwvCjhcwYMJmtMHTt75ixwMs9QqBK281Wy9zeRGVIjRA130_provenance.
- assertion description "[A mechanism for its pathogenesis has not been identified, but loss of function of EXT genes is implicated in sporadic and hereditary multiple osteochondromas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP418015.RAk4I8FiHHhElzhKi4Z5Od-wIDHulV3AUsG5FOajamUP0130_assertion description "[A mechanism for its pathogenesis has not been identified, but loss of function of EXT genes is implicated in sporadic and hereditary multiple osteochondromas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418015.RAk4I8FiHHhElzhKi4Z5Od-wIDHulV3AUsG5FOajamUP0130_provenance.
- NP418017.RAtrKPlwlgIKN2j2QTJJ-kSdnS9Rv1RPsa1OnygotnByQ130_assertion description "[A mechanism for its pathogenesis has not been identified, but loss of function of EXT genes is implicated in sporadic and hereditary multiple osteochondromas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418017.RAtrKPlwlgIKN2j2QTJJ-kSdnS9Rv1RPsa1OnygotnByQ130_provenance.