Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP124839.RAvQHxmOSM0UB2VWR365yQwPCC4nTXgNIDmXP4D79n4Gc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP124839.RAvQHxmOSM0UB2VWR365yQwPCC4nTXgNIDmXP4D79n4Gc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP124839.RAvQHxmOSM0UB2VWR365yQwPCC4nTXgNIDmXP4D79n4Gc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP124839.RAvQHxmOSM0UB2VWR365yQwPCC4nTXgNIDmXP4D79n4Gc130_provenance.
- NP124839.RAvQHxmOSM0UB2VWR365yQwPCC4nTXgNIDmXP4D79n4Gc130_assertion description "[We excluded mutation in 21 biological candidate genes as a common cause of primary lymphedema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP124839.RAvQHxmOSM0UB2VWR365yQwPCC4nTXgNIDmXP4D79n4Gc130_provenance.
- NP124839.RAvQHxmOSM0UB2VWR365yQwPCC4nTXgNIDmXP4D79n4Gc130_assertion evidence source_evidence_literature NP124839.RAvQHxmOSM0UB2VWR365yQwPCC4nTXgNIDmXP4D79n4Gc130_provenance.
- NP124839.RAvQHxmOSM0UB2VWR365yQwPCC4nTXgNIDmXP4D79n4Gc130_assertion SIO_000772 18564921 NP124839.RAvQHxmOSM0UB2VWR365yQwPCC4nTXgNIDmXP4D79n4Gc130_provenance.
- NP124839.RAvQHxmOSM0UB2VWR365yQwPCC4nTXgNIDmXP4D79n4Gc130_assertion wasDerivedFrom gad-20150221 NP124839.RAvQHxmOSM0UB2VWR365yQwPCC4nTXgNIDmXP4D79n4Gc130_provenance.
- NP124839.RAvQHxmOSM0UB2VWR365yQwPCC4nTXgNIDmXP4D79n4Gc130_assertion wasGeneratedBy ECO_0000203 NP124839.RAvQHxmOSM0UB2VWR365yQwPCC4nTXgNIDmXP4D79n4Gc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP124839.RAvQHxmOSM0UB2VWR365yQwPCC4nTXgNIDmXP4D79n4Gc130_provenance.