Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP259733.RAN1uh3aAwYRoS46pI-KVLrP6w3pQLlYi1Oq1gMRj1kmc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP259733.RAN1uh3aAwYRoS46pI-KVLrP6w3pQLlYi1Oq1gMRj1kmc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP259733.RAN1uh3aAwYRoS46pI-KVLrP6w3pQLlYi1Oq1gMRj1kmc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP259733.RAN1uh3aAwYRoS46pI-KVLrP6w3pQLlYi1Oq1gMRj1kmc130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP259733.RAN1uh3aAwYRoS46pI-KVLrP6w3pQLlYi1Oq1gMRj1kmc130_provenance.