Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP829269.RA_OGLUoxQoCn-c4ZCF4l86qbKVo-7Wxfd9XH20VF7vNU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP829269.RA_OGLUoxQoCn-c4ZCF4l86qbKVo-7Wxfd9XH20VF7vNU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP829269.RA_OGLUoxQoCn-c4ZCF4l86qbKVo-7Wxfd9XH20VF7vNU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP829269.RA_OGLUoxQoCn-c4ZCF4l86qbKVo-7Wxfd9XH20VF7vNU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP829269.RA_OGLUoxQoCn-c4ZCF4l86qbKVo-7Wxfd9XH20VF7vNU130_provenance.
- NP829269.RA_OGLUoxQoCn-c4ZCF4l86qbKVo-7Wxfd9XH20VF7vNU130_assertion wasGeneratedBy ECO_0000203 NP829269.RA_OGLUoxQoCn-c4ZCF4l86qbKVo-7Wxfd9XH20VF7vNU130_provenance.
- NP829269.RA_OGLUoxQoCn-c4ZCF4l86qbKVo-7Wxfd9XH20VF7vNU130_assertion wasDerivedFrom befree-20150227 NP829269.RA_OGLUoxQoCn-c4ZCF4l86qbKVo-7Wxfd9XH20VF7vNU130_provenance.
- NP829269.RA_OGLUoxQoCn-c4ZCF4l86qbKVo-7Wxfd9XH20VF7vNU130_assertion SIO_000772 19396027 NP829269.RA_OGLUoxQoCn-c4ZCF4l86qbKVo-7Wxfd9XH20VF7vNU130_provenance.
- NP829269.RA_OGLUoxQoCn-c4ZCF4l86qbKVo-7Wxfd9XH20VF7vNU130_assertion evidence source_evidence_literature NP829269.RA_OGLUoxQoCn-c4ZCF4l86qbKVo-7Wxfd9XH20VF7vNU130_provenance.
- NP829269.RA_OGLUoxQoCn-c4ZCF4l86qbKVo-7Wxfd9XH20VF7vNU130_assertion description "[More recently, we have identified ADAMTSL2 mutations in GD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP829269.RA_OGLUoxQoCn-c4ZCF4l86qbKVo-7Wxfd9XH20VF7vNU130_provenance.