Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[A novel microduplication syndrome involving various-sized contiguous duplications in 17p13.3 has recently been described, suggesting that increased copy number of genes in 17p13.3, particularly PAFAH1B1, is associated with clinical features including facial dysmorphism, developmental delay, and autism spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP545115.RASmXtn9l92KTXtdcAVQGeQ0IPyj8T3Tw5XW1P9Oq0D8E130_assertion description "[A novel microduplication syndrome involving various-sized contiguous duplications in 17p13.3 has recently been described, suggesting that increased copy number of genes in 17p13.3, particularly PAFAH1B1, is associated with clinical features including facial dysmorphism, developmental delay, and autism spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP545115.RASmXtn9l92KTXtdcAVQGeQ0IPyj8T3Tw5XW1P9Oq0D8E130_provenance.
• NP448531.RAhID7yCGMZpCYbp4ad6yK8HF_xJPGbu7yTw8MbMHw_EY130_assertion description "[A novel microduplication syndrome involving various-sized contiguous duplications in 17p13.3 has recently been described, suggesting that increased copy number of genes in 17p13.3, particularly PAFAH1B1, is associated with clinical features including facial dysmorphism, developmental delay, and autism spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP448531.RAhID7yCGMZpCYbp4ad6yK8HF_xJPGbu7yTw8MbMHw_EY130_provenance.
• NP488690.RAMI1aj8wDHZI3TuwRRqv1mDx_yCtOOGfcaZVQIR10Y5E130_assertion description "[A novel microduplication syndrome involving various-sized contiguous duplications in 17p13.3 has recently been described, suggesting that increased copy number of genes in 17p13.3, particularly PAFAH1B1, is associated with clinical features including facial dysmorphism, developmental delay, and autism spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP488690.RAMI1aj8wDHZI3TuwRRqv1mDx_yCtOOGfcaZVQIR10Y5E130_provenance.
• assertion description "[A novel microduplication syndrome involving various-sized contiguous duplications in 17p13.3 has recently been described, suggesting that increased copy number of genes in 17p13.3, particularly PAFAH1B1, is associated with clinical features including facial dysmorphism, developmental delay, and autism spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[A novel microduplication syndrome involving various-sized contiguous duplications in 17p13.3 has recently been described, suggesting that increased copy number of genes in 17p13.3, particularly PAFAH1B1, is associated with clinical features including facial dysmorphism, developmental delay, and autism spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[A novel microduplication syndrome involving various-sized contiguous duplications in 17p13.3 has recently been described, suggesting that increased copy number of genes in 17p13.3, particularly PAFAH1B1, is associated with clinical features including facial dysmorphism, developmental delay, and autism spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP922147.RARotScJijlmuWgSGEdgbPLybtW21uGgJIu5U4nsPf1bQ130_assertion description "[A novel microduplication syndrome involving various-sized contiguous duplications in 17p13.3 has recently been described, suggesting that increased copy number of genes in 17p13.3, particularly PAFAH1B1, is associated with clinical features including facial dysmorphism, developmental delay, and autism spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP922147.RARotScJijlmuWgSGEdgbPLybtW21uGgJIu5U4nsPf1bQ130_provenance.
• NP606085.RABlnjIL_HglBy_2WUS25haV1Z1TGFhpyszWYVf9BuKSw130_assertion description "[A novel microduplication syndrome involving various-sized contiguous duplications in 17p13.3 has recently been described, suggesting that increased copy number of genes in 17p13.3, particularly PAFAH1B1, is associated with clinical features including facial dysmorphism, developmental delay, and autism spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606085.RABlnjIL_HglBy_2WUS25haV1Z1TGFhpyszWYVf9BuKSw130_provenance.
• NP922146.RAtTYDamCrY44pe2EHhFqbn4Y7GQ7Tpm8NL8Akln_cfAc130_assertion description "[A novel microduplication syndrome involving various-sized contiguous duplications in 17p13.3 has recently been described, suggesting that increased copy number of genes in 17p13.3, particularly PAFAH1B1, is associated with clinical features including facial dysmorphism, developmental delay, and autism spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP922146.RAtTYDamCrY44pe2EHhFqbn4Y7GQ7Tpm8NL8Akln_cfAc130_provenance.
• NP606182.RAwOqDab0u9g1GaEn5-EfWcYX21uPXAHFVdrC1JVVP5Vc130_assertion description "[A novel microduplication syndrome involving various-sized contiguous duplications in 17p13.3 has recently been described, suggesting that increased copy number of genes in 17p13.3, particularly PAFAH1B1, is associated with clinical features including facial dysmorphism, developmental delay, and autism spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606182.RAwOqDab0u9g1GaEn5-EfWcYX21uPXAHFVdrC1JVVP5Vc130_provenance.