Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1376016.RAHBxhSGQMzTBBSrIMqVJhxXzS81v4hJOd1KRSFyWm7o4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1376016.RAHBxhSGQMzTBBSrIMqVJhxXzS81v4hJOd1KRSFyWm7o4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1376016.RAHBxhSGQMzTBBSrIMqVJhxXzS81v4hJOd1KRSFyWm7o4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1376016.RAHBxhSGQMzTBBSrIMqVJhxXzS81v4hJOd1KRSFyWm7o4130_provenance.
- NP1376016.RAHBxhSGQMzTBBSrIMqVJhxXzS81v4hJOd1KRSFyWm7o4130_assertion description "[Thus, these results together suggest that CCD is produced by haploinsufficiency of OSF2/CBFA1 and provide direct genetic evidence that the phenotype is secondary to an alteration of osteoblast differentiation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1376016.RAHBxhSGQMzTBBSrIMqVJhxXzS81v4hJOd1KRSFyWm7o4130_provenance.
- NP1376016.RAHBxhSGQMzTBBSrIMqVJhxXzS81v4hJOd1KRSFyWm7o4130_assertion evidence source_evidence_literature NP1376016.RAHBxhSGQMzTBBSrIMqVJhxXzS81v4hJOd1KRSFyWm7o4130_provenance.
- NP1376016.RAHBxhSGQMzTBBSrIMqVJhxXzS81v4hJOd1KRSFyWm7o4130_assertion SIO_000772 9207800 NP1376016.RAHBxhSGQMzTBBSrIMqVJhxXzS81v4hJOd1KRSFyWm7o4130_provenance.
- NP1376016.RAHBxhSGQMzTBBSrIMqVJhxXzS81v4hJOd1KRSFyWm7o4130_assertion wasDerivedFrom befree-2016 NP1376016.RAHBxhSGQMzTBBSrIMqVJhxXzS81v4hJOd1KRSFyWm7o4130_provenance.
- NP1376016.RAHBxhSGQMzTBBSrIMqVJhxXzS81v4hJOd1KRSFyWm7o4130_assertion wasGeneratedBy ECO_0000203 NP1376016.RAHBxhSGQMzTBBSrIMqVJhxXzS81v4hJOd1KRSFyWm7o4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1376016.RAHBxhSGQMzTBBSrIMqVJhxXzS81v4hJOd1KRSFyWm7o4130_provenance.