Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP583706.RAOcCPY7kVJlmlG_Wvxp1NJkHgj3gyD_u7qmfpAWycjA4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP583706.RAOcCPY7kVJlmlG_Wvxp1NJkHgj3gyD_u7qmfpAWycjA4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583706.RAOcCPY7kVJlmlG_Wvxp1NJkHgj3gyD_u7qmfpAWycjA4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583706.RAOcCPY7kVJlmlG_Wvxp1NJkHgj3gyD_u7qmfpAWycjA4130_provenance.
- NP583706.RAOcCPY7kVJlmlG_Wvxp1NJkHgj3gyD_u7qmfpAWycjA4130_assertion description "[Autosomal dominant craniometaphyseal dysplasia is caused by mutations in the transmembrane protein ANK.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583706.RAOcCPY7kVJlmlG_Wvxp1NJkHgj3gyD_u7qmfpAWycjA4130_provenance.
- NP583706.RAOcCPY7kVJlmlG_Wvxp1NJkHgj3gyD_u7qmfpAWycjA4130_assertion evidence source_evidence_literature NP583706.RAOcCPY7kVJlmlG_Wvxp1NJkHgj3gyD_u7qmfpAWycjA4130_provenance.
- NP583706.RAOcCPY7kVJlmlG_Wvxp1NJkHgj3gyD_u7qmfpAWycjA4130_assertion SIO_000772 11326338 NP583706.RAOcCPY7kVJlmlG_Wvxp1NJkHgj3gyD_u7qmfpAWycjA4130_provenance.
- NP583706.RAOcCPY7kVJlmlG_Wvxp1NJkHgj3gyD_u7qmfpAWycjA4130_assertion wasDerivedFrom befree-20140225 NP583706.RAOcCPY7kVJlmlG_Wvxp1NJkHgj3gyD_u7qmfpAWycjA4130_provenance.
- NP583706.RAOcCPY7kVJlmlG_Wvxp1NJkHgj3gyD_u7qmfpAWycjA4130_assertion wasGeneratedBy ECO_0000203 NP583706.RAOcCPY7kVJlmlG_Wvxp1NJkHgj3gyD_u7qmfpAWycjA4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP583706.RAOcCPY7kVJlmlG_Wvxp1NJkHgj3gyD_u7qmfpAWycjA4130_provenance.