Matches in Nanopublications for { ?s ?p "[Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA-PLA1alpha in autosomal recessive hypotrichosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP921460.RAqXdy_6X3QR0z2NN-Jqux_ZDDY0ulCvtzsXqam9SRThs130_assertion description "[Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA-PLA1alpha in autosomal recessive hypotrichosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921460.RAqXdy_6X3QR0z2NN-Jqux_ZDDY0ulCvtzsXqam9SRThs130_provenance.
- NP245716.RAHzUkMQHxjI8-zFFkuCtfLQK9hYZFRy6geXKUV0lkE7M130_assertion description "[Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA-PLA1alpha in autosomal recessive hypotrichosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP245716.RAHzUkMQHxjI8-zFFkuCtfLQK9hYZFRy6geXKUV0lkE7M130_provenance.
- NP841706.RATWmgAwUtbGBRo35I1mSuzUG_0LuawVr5pfigiAlA7rw130_assertion description "[Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA-PLA1alpha in autosomal recessive hypotrichosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841706.RATWmgAwUtbGBRo35I1mSuzUG_0LuawVr5pfigiAlA7rw130_provenance.
- assertion description "[Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA-PLA1alpha in autosomal recessive hypotrichosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP798696.RAbmHYOLUwT-x-csEVfq9HgCq6KShS9dKuVQ-E4VNE0-k130_assertion description "[Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA-PLA1alpha in autosomal recessive hypotrichosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP798696.RAbmHYOLUwT-x-csEVfq9HgCq6KShS9dKuVQ-E4VNE0-k130_provenance.
- NP837756.RA7DUjxH4vFZwhtceWVWSIUjH516KgQkJ9tQ70TO3Z2J8130_assertion description "[Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA-PLA1alpha in autosomal recessive hypotrichosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837756.RA7DUjxH4vFZwhtceWVWSIUjH516KgQkJ9tQ70TO3Z2J8130_provenance.