Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP142429.RAwcpzJM4QlF4xDzMheD9hpKcK1blsyxtYEkPGAayE-LE130_assertion> ?p ?o ?g. }
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- NP142429.RAwcpzJM4QlF4xDzMheD9hpKcK1blsyxtYEkPGAayE-LE130_assertion type Assertion NP142429.RAwcpzJM4QlF4xDzMheD9hpKcK1blsyxtYEkPGAayE-LE130_head.
- NP142429.RAwcpzJM4QlF4xDzMheD9hpKcK1blsyxtYEkPGAayE-LE130_assertion wasGeneratedBy ECO_0000203 NP142429.RAwcpzJM4QlF4xDzMheD9hpKcK1blsyxtYEkPGAayE-LE130_provenance.
- NP142429.RAwcpzJM4QlF4xDzMheD9hpKcK1blsyxtYEkPGAayE-LE130_assertion wasDerivedFrom gad-20150221 NP142429.RAwcpzJM4QlF4xDzMheD9hpKcK1blsyxtYEkPGAayE-LE130_provenance.
- NP142429.RAwcpzJM4QlF4xDzMheD9hpKcK1blsyxtYEkPGAayE-LE130_assertion SIO_000772 20531469 NP142429.RAwcpzJM4QlF4xDzMheD9hpKcK1blsyxtYEkPGAayE-LE130_provenance.
- NP142429.RAwcpzJM4QlF4xDzMheD9hpKcK1blsyxtYEkPGAayE-LE130_assertion evidence source_evidence_literature NP142429.RAwcpzJM4QlF4xDzMheD9hpKcK1blsyxtYEkPGAayE-LE130_provenance.
- NP142429.RAwcpzJM4QlF4xDzMheD9hpKcK1blsyxtYEkPGAayE-LE130_assertion description "[Functional impact of global rare copy number variation in autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP142429.RAwcpzJM4QlF4xDzMheD9hpKcK1blsyxtYEkPGAayE-LE130_provenance.