Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP941701.RAV9eFVqDuudVQTY57JZqgWR9vn4HT--RdjEDeRJ4vdJs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP941701.RAV9eFVqDuudVQTY57JZqgWR9vn4HT--RdjEDeRJ4vdJs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP941701.RAV9eFVqDuudVQTY57JZqgWR9vn4HT--RdjEDeRJ4vdJs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP941701.RAV9eFVqDuudVQTY57JZqgWR9vn4HT--RdjEDeRJ4vdJs130_provenance.
- NP941701.RAV9eFVqDuudVQTY57JZqgWR9vn4HT--RdjEDeRJ4vdJs130_assertion description "[Here, we described that homozygous mutations in EXT1/EXT2, which are causative for osteochondroma formation, are likely to affect terminal chondrocyte differentiation and vascularisation in the osteocartilaginous interface.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP941701.RAV9eFVqDuudVQTY57JZqgWR9vn4HT--RdjEDeRJ4vdJs130_provenance.
- NP941701.RAV9eFVqDuudVQTY57JZqgWR9vn4HT--RdjEDeRJ4vdJs130_assertion evidence source_evidence_literature NP941701.RAV9eFVqDuudVQTY57JZqgWR9vn4HT--RdjEDeRJ4vdJs130_provenance.
- NP941701.RAV9eFVqDuudVQTY57JZqgWR9vn4HT--RdjEDeRJ4vdJs130_assertion SIO_000772 22116208 NP941701.RAV9eFVqDuudVQTY57JZqgWR9vn4HT--RdjEDeRJ4vdJs130_provenance.
- NP941701.RAV9eFVqDuudVQTY57JZqgWR9vn4HT--RdjEDeRJ4vdJs130_assertion wasDerivedFrom befree-2016 NP941701.RAV9eFVqDuudVQTY57JZqgWR9vn4HT--RdjEDeRJ4vdJs130_provenance.
- NP941701.RAV9eFVqDuudVQTY57JZqgWR9vn4HT--RdjEDeRJ4vdJs130_assertion wasGeneratedBy ECO_0000203 NP941701.RAV9eFVqDuudVQTY57JZqgWR9vn4HT--RdjEDeRJ4vdJs130_provenance.
- befree-2016 importedOn "2016-02-19" NP941701.RAV9eFVqDuudVQTY57JZqgWR9vn4HT--RdjEDeRJ4vdJs130_provenance.