Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP699926.RASTTAKNAW-NpZ4NJuCeP4hWqxT1ED_8AHZBlsJ1Jm-7o130_assertion description "[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699926.RASTTAKNAW-NpZ4NJuCeP4hWqxT1ED_8AHZBlsJ1Jm-7o130_provenance.
• NP169994.RAYsJELbCUGuiNPle66DkUBkUDPsW539MRgRjNGI-hYrk130_assertion description "[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP169994.RAYsJELbCUGuiNPle66DkUBkUDPsW539MRgRjNGI-hYrk130_provenance.
• NP685904.RAjbDMNVgiWnL7ugF8z-FG8Kr1rXO0iwLxx1IpRB_KGuY130_assertion description "[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP685904.RAjbDMNVgiWnL7ugF8z-FG8Kr1rXO0iwLxx1IpRB_KGuY130_provenance.
• NP318831.RA7_b5A6Wx9JqDnOZ7b21Na73QUXhhoR0HRRmy84LKcsM130_assertion description "[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP318831.RA7_b5A6Wx9JqDnOZ7b21Na73QUXhhoR0HRRmy84LKcsM130_provenance.
• NP832388.RA4zsHkwwZZ6DvJx5b0yltsu2OsPrmRlQZsWbZ9xSFbpU130_assertion description "[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP832388.RA4zsHkwwZZ6DvJx5b0yltsu2OsPrmRlQZsWbZ9xSFbpU130_provenance.
• NP950313.RAUgeweyXWlU_la8NgEFckJ25BG5QEqX75YtAIxxQoZIw130_assertion description "[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP950313.RAUgeweyXWlU_la8NgEFckJ25BG5QEqX75YtAIxxQoZIw130_provenance.
• NP881289.RA_eCvJyZo0HyHJ167Sou-UNQaC2KTPKuo4sXOE5RveTU130_assertion description "[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881289.RA_eCvJyZo0HyHJ167Sou-UNQaC2KTPKuo4sXOE5RveTU130_provenance.
• NP1035059.RAxPz1YWztWwmKTbs9FA0gYE-g3jI69KCEnvJzXwMtPpY130_assertion description "[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1035059.RAxPz1YWztWwmKTbs9FA0gYE-g3jI69KCEnvJzXwMtPpY130_provenance.
• NP1035060.RAw113I3_c87D0sBjq6lZ5kZyrGixatDngVH8YkeacP0c130_assertion description "[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1035060.RAw113I3_c87D0sBjq6lZ5kZyrGixatDngVH8YkeacP0c130_provenance.
• assertion description "[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP962535.RAv1Eoj7-E4RUY-WmpTE2GCMeopMcZzfodVEgG6IuSEq0130_assertion description "[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP962535.RAv1Eoj7-E4RUY-WmpTE2GCMeopMcZzfodVEgG6IuSEq0130_provenance.
• assertion description "[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1035058.RAFNDZwbWIe7yZjwDlnUxHzWVrgP7FvfIgltIaDLLepyQ130_assertion description "[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1035058.RAFNDZwbWIe7yZjwDlnUxHzWVrgP7FvfIgltIaDLLepyQ130_provenance.
• NP1035061.RAoVKW1RLh3nP9jWS-aazAMmNoGGWGxK7r1T4YyP4uwDc130_assertion description "[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1035061.RAoVKW1RLh3nP9jWS-aazAMmNoGGWGxK7r1T4YyP4uwDc130_provenance.