Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP26961.RAWrI8sBJTOGNLkfTn0usUArVn8ZBBSSYXQ8nqQdWPrGM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP26961.RAWrI8sBJTOGNLkfTn0usUArVn8ZBBSSYXQ8nqQdWPrGM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP26961.RAWrI8sBJTOGNLkfTn0usUArVn8ZBBSSYXQ8nqQdWPrGM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP26961.RAWrI8sBJTOGNLkfTn0usUArVn8ZBBSSYXQ8nqQdWPrGM130_provenance.
- NP26961.RAWrI8sBJTOGNLkfTn0usUArVn8ZBBSSYXQ8nqQdWPrGM130_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." NP26961.RAWrI8sBJTOGNLkfTn0usUArVn8ZBBSSYXQ8nqQdWPrGM130_provenance.
- NP26961.RAWrI8sBJTOGNLkfTn0usUArVn8ZBBSSYXQ8nqQdWPrGM130_assertion evidence source_evidence_curated NP26961.RAWrI8sBJTOGNLkfTn0usUArVn8ZBBSSYXQ8nqQdWPrGM130_provenance.
- NP26961.RAWrI8sBJTOGNLkfTn0usUArVn8ZBBSSYXQ8nqQdWPrGM130_assertion SIO_000772 16740914 NP26961.RAWrI8sBJTOGNLkfTn0usUArVn8ZBBSSYXQ8nqQdWPrGM130_provenance.
- NP26961.RAWrI8sBJTOGNLkfTn0usUArVn8ZBBSSYXQ8nqQdWPrGM130_assertion wasDerivedFrom ctd_human-20150221 NP26961.RAWrI8sBJTOGNLkfTn0usUArVn8ZBBSSYXQ8nqQdWPrGM130_provenance.
- NP26961.RAWrI8sBJTOGNLkfTn0usUArVn8ZBBSSYXQ8nqQdWPrGM130_assertion wasGeneratedBy ECO_0000218 NP26961.RAWrI8sBJTOGNLkfTn0usUArVn8ZBBSSYXQ8nqQdWPrGM130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP26961.RAWrI8sBJTOGNLkfTn0usUArVn8ZBBSSYXQ8nqQdWPrGM130_provenance.