Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_provenance.
- NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_assertion wasGeneratedBy ECO_0000203 NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_provenance.
- NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_assertion wasDerivedFrom befree-20140225 NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_provenance.
- NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_assertion SIO_000772 22152678 NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_provenance.
- NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_assertion evidence source_evidence_literature NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_provenance.
- NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_assertion description "[We used whole-exome sequencing of five unrelated individuals with lepto-SEMDJL to identify mutations in KIF22 as the cause of this skeletal condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_provenance.