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Matches in Nanopublications for { ?s ?p "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP919411.RAYxu3AjqKbCbi7c81-NL40ZMauvoQ6SupkaJIIONdppw130_assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919411.RAYxu3AjqKbCbi7c81-NL40ZMauvoQ6SupkaJIIONdppw130_provenance.
• NP799711.RAwhTZGklK0cR3J1gIdC4EVtqR2jbgDj-zL3q06L4ZzUI130_assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799711.RAwhTZGklK0cR3J1gIdC4EVtqR2jbgDj-zL3q06L4ZzUI130_provenance.
• NP761981.RA-yUZ3c_WF4PkhhIwy9xElJB9gl_7enz6v0sXtUBzq_c130_assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761981.RA-yUZ3c_WF4PkhhIwy9xElJB9gl_7enz6v0sXtUBzq_c130_provenance.
• assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP953423.RAnF22Z4N7BJMybQPEwfx-BzbivH4L6qPW8BkH3Zp0Ra4130_assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP953423.RAnF22Z4N7BJMybQPEwfx-BzbivH4L6qPW8BkH3Zp0Ra4130_provenance.
• assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP771462.RAm_ElcflHm2AKB4Bg1wSHXnQvn6MBZSknuws2eRPC2Q0130_assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771462.RAm_ElcflHm2AKB4Bg1wSHXnQvn6MBZSknuws2eRPC2Q0130_provenance.
• NP771463.RAij0mU3SZkTu8-Qut2kfwTeGy_vhR4xphf7zC2UNrJXc130_assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771463.RAij0mU3SZkTu8-Qut2kfwTeGy_vhR4xphf7zC2UNrJXc130_provenance.
• NP857420.RAOj7aqjsuOY8GMTgPK8tAX0kC8lD1Ves-owmFVOqDSHQ130_assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857420.RAOj7aqjsuOY8GMTgPK8tAX0kC8lD1Ves-owmFVOqDSHQ130_provenance.
• NP771465.RAOelkeZja0PVMNTdYUSZhBNj3Beyz19lhjEHFdjeQSdI130_assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771465.RAOelkeZja0PVMNTdYUSZhBNj3Beyz19lhjEHFdjeQSdI130_provenance.
• NP953432.RAwzM8y_jqOqjQ7aYhkm4kGHcloqEPK9fkhJSrzM01iq0130_assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP953432.RAwzM8y_jqOqjQ7aYhkm4kGHcloqEPK9fkhJSrzM01iq0130_provenance.
• NP771461.RA7KtnKMvJJSupuTrYxVOqGAhzoU2WJwBlLquFaIOr_tE130_assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771461.RA7KtnKMvJJSupuTrYxVOqGAhzoU2WJwBlLquFaIOr_tE130_provenance.