Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Mutations in NPHS1, which encodes nephrin, are the main causes of congenital nephrotic syndrome (CNS) in Finnish patients, whereas mutations in NPHS2, which encodes podocin, are typically responsible for childhood-onset steroid-resistant nephrotic syndrome in European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP294592.RAl3NWqiURZ52jj_vngaByANAgQbnunB-iMRjM1SyCrlw130_assertion description "[Mutations in NPHS1, which encodes nephrin, are the main causes of congenital nephrotic syndrome (CNS) in Finnish patients, whereas mutations in NPHS2, which encodes podocin, are typically responsible for childhood-onset steroid-resistant nephrotic syndrome in European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294592.RAl3NWqiURZ52jj_vngaByANAgQbnunB-iMRjM1SyCrlw130_provenance.
• NP778712.RA_qMFeQK9MDiPmqMOUYlilggq3YvV9BbT4WTCIP6sS5s130_assertion description "[Mutations in NPHS1, which encodes nephrin, are the main causes of congenital nephrotic syndrome (CNS) in Finnish patients, whereas mutations in NPHS2, which encodes podocin, are typically responsible for childhood-onset steroid-resistant nephrotic syndrome in European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778712.RA_qMFeQK9MDiPmqMOUYlilggq3YvV9BbT4WTCIP6sS5s130_provenance.
• NP597417.RAW0xm3_ECJYQvao_CSqJaCyj4kbJ-Lm_bCHIT1GgnJwk130_assertion description "[Mutations in NPHS1, which encodes nephrin, are the main causes of congenital nephrotic syndrome (CNS) in Finnish patients, whereas mutations in NPHS2, which encodes podocin, are typically responsible for childhood-onset steroid-resistant nephrotic syndrome in European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597417.RAW0xm3_ECJYQvao_CSqJaCyj4kbJ-Lm_bCHIT1GgnJwk130_provenance.
• NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_assertion description "[Mutations in NPHS1, which encodes nephrin, are the main causes of congenital nephrotic syndrome (CNS) in Finnish patients, whereas mutations in NPHS2, which encodes podocin, are typically responsible for childhood-onset steroid-resistant nephrotic syndrome in European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_provenance.
• assertion description "[Mutations in NPHS1, which encodes nephrin, are the main causes of congenital nephrotic syndrome (CNS) in Finnish patients, whereas mutations in NPHS2, which encodes podocin, are typically responsible for childhood-onset steroid-resistant nephrotic syndrome in European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in NPHS1, which encodes nephrin, are the main causes of congenital nephrotic syndrome (CNS) in Finnish patients, whereas mutations in NPHS2, which encodes podocin, are typically responsible for childhood-onset steroid-resistant nephrotic syndrome in European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in NPHS1, which encodes nephrin, are the main causes of congenital nephrotic syndrome (CNS) in Finnish patients, whereas mutations in NPHS2, which encodes podocin, are typically responsible for childhood-onset steroid-resistant nephrotic syndrome in European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in NPHS1, which encodes nephrin, are the main causes of congenital nephrotic syndrome (CNS) in Finnish patients, whereas mutations in NPHS2, which encodes podocin, are typically responsible for childhood-onset steroid-resistant nephrotic syndrome in European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in NPHS1, which encodes nephrin, are the main causes of congenital nephrotic syndrome (CNS) in Finnish patients, whereas mutations in NPHS2, which encodes podocin, are typically responsible for childhood-onset steroid-resistant nephrotic syndrome in European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in NPHS1, which encodes nephrin, are the main causes of congenital nephrotic syndrome (CNS) in Finnish patients, whereas mutations in NPHS2, which encodes podocin, are typically responsible for childhood-onset steroid-resistant nephrotic syndrome in European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP783760.RAu7zHfJ-hdn_iqqlgPuWjISZRfFOcO7riX2KzRBhIoaQ130_assertion description "[Mutations in NPHS1, which encodes nephrin, are the main causes of congenital nephrotic syndrome (CNS) in Finnish patients, whereas mutations in NPHS2, which encodes podocin, are typically responsible for childhood-onset steroid-resistant nephrotic syndrome in European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783760.RAu7zHfJ-hdn_iqqlgPuWjISZRfFOcO7riX2KzRBhIoaQ130_provenance.
• NP807881.RAKPWC8A3CoJaF8q2CyvIlpgpmXqKrkAfr9HlTaQgpj9w130_assertion description "[Mutations in NPHS1, which encodes nephrin, are the main causes of congenital nephrotic syndrome (CNS) in Finnish patients, whereas mutations in NPHS2, which encodes podocin, are typically responsible for childhood-onset steroid-resistant nephrotic syndrome in European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP807881.RAKPWC8A3CoJaF8q2CyvIlpgpmXqKrkAfr9HlTaQgpj9w130_provenance.
• NP815298.RAtiGxlK9RBWx9MSpE6pG8cp-qADhEBif2yL7eT9LETGc130_assertion description "[Mutations in NPHS1, which encodes nephrin, are the main causes of congenital nephrotic syndrome (CNS) in Finnish patients, whereas mutations in NPHS2, which encodes podocin, are typically responsible for childhood-onset steroid-resistant nephrotic syndrome in European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP815298.RAtiGxlK9RBWx9MSpE6pG8cp-qADhEBif2yL7eT9LETGc130_provenance.
• NP815299.RApPfeeJFebpUrTUgljv_DolDPv-6ntIXfVxWrD3CThNk130_assertion description "[Mutations in NPHS1, which encodes nephrin, are the main causes of congenital nephrotic syndrome (CNS) in Finnish patients, whereas mutations in NPHS2, which encodes podocin, are typically responsible for childhood-onset steroid-resistant nephrotic syndrome in European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP815299.RApPfeeJFebpUrTUgljv_DolDPv-6ntIXfVxWrD3CThNk130_provenance.