Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP516760.RAjVfHbztxtjAMBB9xVIsur70I_KrettJubQq6VWa_nH0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP516760.RAjVfHbztxtjAMBB9xVIsur70I_KrettJubQq6VWa_nH0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP516760.RAjVfHbztxtjAMBB9xVIsur70I_KrettJubQq6VWa_nH0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP516760.RAjVfHbztxtjAMBB9xVIsur70I_KrettJubQq6VWa_nH0130_provenance.
- NP516760.RAjVfHbztxtjAMBB9xVIsur70I_KrettJubQq6VWa_nH0130_assertion description "[The clinical similarity of our family to these patients with mutations in PQBP1, particularly the presence of microcephaly, short stature, and atrial septal defect, prompted examination of this gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP516760.RAjVfHbztxtjAMBB9xVIsur70I_KrettJubQq6VWa_nH0130_provenance.
- NP516760.RAjVfHbztxtjAMBB9xVIsur70I_KrettJubQq6VWa_nH0130_assertion evidence source_evidence_literature NP516760.RAjVfHbztxtjAMBB9xVIsur70I_KrettJubQq6VWa_nH0130_provenance.
- NP516760.RAjVfHbztxtjAMBB9xVIsur70I_KrettJubQq6VWa_nH0130_assertion SIO_000772 16740914 NP516760.RAjVfHbztxtjAMBB9xVIsur70I_KrettJubQq6VWa_nH0130_provenance.
- NP516760.RAjVfHbztxtjAMBB9xVIsur70I_KrettJubQq6VWa_nH0130_assertion wasDerivedFrom befree-20140225 NP516760.RAjVfHbztxtjAMBB9xVIsur70I_KrettJubQq6VWa_nH0130_provenance.
- NP516760.RAjVfHbztxtjAMBB9xVIsur70I_KrettJubQq6VWa_nH0130_assertion wasGeneratedBy ECO_0000203 NP516760.RAjVfHbztxtjAMBB9xVIsur70I_KrettJubQq6VWa_nH0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP516760.RAjVfHbztxtjAMBB9xVIsur70I_KrettJubQq6VWa_nH0130_provenance.