Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP156370.RAD7hpq83f0QUvXTZ6eiyuTt8AlO8HWRkqnKz-syDLzDQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP156370.RAD7hpq83f0QUvXTZ6eiyuTt8AlO8HWRkqnKz-syDLzDQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP156370.RAD7hpq83f0QUvXTZ6eiyuTt8AlO8HWRkqnKz-syDLzDQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP156370.RAD7hpq83f0QUvXTZ6eiyuTt8AlO8HWRkqnKz-syDLzDQ130_provenance.
- NP156370.RAD7hpq83f0QUvXTZ6eiyuTt8AlO8HWRkqnKz-syDLzDQ130_assertion description "[Ehlers-Danlos syndrome type IV: unusual congenital anomalies in a mother and son with a COL3A1 mutation and a normal collagen III protein profile.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP156370.RAD7hpq83f0QUvXTZ6eiyuTt8AlO8HWRkqnKz-syDLzDQ130_provenance.
- NP156370.RAD7hpq83f0QUvXTZ6eiyuTt8AlO8HWRkqnKz-syDLzDQ130_assertion evidence source_evidence_literature NP156370.RAD7hpq83f0QUvXTZ6eiyuTt8AlO8HWRkqnKz-syDLzDQ130_provenance.
- NP156370.RAD7hpq83f0QUvXTZ6eiyuTt8AlO8HWRkqnKz-syDLzDQ130_assertion SIO_000772 12694234 NP156370.RAD7hpq83f0QUvXTZ6eiyuTt8AlO8HWRkqnKz-syDLzDQ130_provenance.
- NP156370.RAD7hpq83f0QUvXTZ6eiyuTt8AlO8HWRkqnKz-syDLzDQ130_assertion wasDerivedFrom befree-20140225 NP156370.RAD7hpq83f0QUvXTZ6eiyuTt8AlO8HWRkqnKz-syDLzDQ130_provenance.
- NP156370.RAD7hpq83f0QUvXTZ6eiyuTt8AlO8HWRkqnKz-syDLzDQ130_assertion wasGeneratedBy ECO_0000203 NP156370.RAD7hpq83f0QUvXTZ6eiyuTt8AlO8HWRkqnKz-syDLzDQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP156370.RAD7hpq83f0QUvXTZ6eiyuTt8AlO8HWRkqnKz-syDLzDQ130_provenance.