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- NP259733.RAN1uh3aAwYRoS46pI-KVLrP6w3pQLlYi1Oq1gMRj1kmc130_assertion type Assertion NP259733.RAN1uh3aAwYRoS46pI-KVLrP6w3pQLlYi1Oq1gMRj1kmc130_head.
- NP259733.RAN1uh3aAwYRoS46pI-KVLrP6w3pQLlYi1Oq1gMRj1kmc130_assertion description "[Here, we report the identification of a founder mutation in the BBS2 gene as the cause for the increased incidence of this developmental disorder in the Hutterite population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259733.RAN1uh3aAwYRoS46pI-KVLrP6w3pQLlYi1Oq1gMRj1kmc130_provenance.
- NP259733.RAN1uh3aAwYRoS46pI-KVLrP6w3pQLlYi1Oq1gMRj1kmc130_assertion evidence source_evidence_literature NP259733.RAN1uh3aAwYRoS46pI-KVLrP6w3pQLlYi1Oq1gMRj1kmc130_provenance.
- NP259733.RAN1uh3aAwYRoS46pI-KVLrP6w3pQLlYi1Oq1gMRj1kmc130_assertion SIO_000772 20618352 NP259733.RAN1uh3aAwYRoS46pI-KVLrP6w3pQLlYi1Oq1gMRj1kmc130_provenance.
- NP259733.RAN1uh3aAwYRoS46pI-KVLrP6w3pQLlYi1Oq1gMRj1kmc130_assertion wasDerivedFrom befree-20150227 NP259733.RAN1uh3aAwYRoS46pI-KVLrP6w3pQLlYi1Oq1gMRj1kmc130_provenance.
- NP259733.RAN1uh3aAwYRoS46pI-KVLrP6w3pQLlYi1Oq1gMRj1kmc130_assertion wasGeneratedBy ECO_0000203 NP259733.RAN1uh3aAwYRoS46pI-KVLrP6w3pQLlYi1Oq1gMRj1kmc130_provenance.