Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP219803.RAUTAD_obKWj2MjSV9GhwSfwX9ciNIi2kuf3U-bu8eq_k130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP219803.RAUTAD_obKWj2MjSV9GhwSfwX9ciNIi2kuf3U-bu8eq_k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP219803.RAUTAD_obKWj2MjSV9GhwSfwX9ciNIi2kuf3U-bu8eq_k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP219803.RAUTAD_obKWj2MjSV9GhwSfwX9ciNIi2kuf3U-bu8eq_k130_provenance.
- NP219803.RAUTAD_obKWj2MjSV9GhwSfwX9ciNIi2kuf3U-bu8eq_k130_assertion description "[Furthermore, PRRT2 mutations elicit pleiotropy in terms of both age of expression (infancy versus later childhood) and anatomical substrate (cortex versus basal ganglia).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP219803.RAUTAD_obKWj2MjSV9GhwSfwX9ciNIi2kuf3U-bu8eq_k130_provenance.
- NP219803.RAUTAD_obKWj2MjSV9GhwSfwX9ciNIi2kuf3U-bu8eq_k130_assertion evidence source_evidence_literature NP219803.RAUTAD_obKWj2MjSV9GhwSfwX9ciNIi2kuf3U-bu8eq_k130_provenance.
- NP219803.RAUTAD_obKWj2MjSV9GhwSfwX9ciNIi2kuf3U-bu8eq_k130_assertion SIO_000772 22243967 NP219803.RAUTAD_obKWj2MjSV9GhwSfwX9ciNIi2kuf3U-bu8eq_k130_provenance.
- NP219803.RAUTAD_obKWj2MjSV9GhwSfwX9ciNIi2kuf3U-bu8eq_k130_assertion wasDerivedFrom befree-20140225 NP219803.RAUTAD_obKWj2MjSV9GhwSfwX9ciNIi2kuf3U-bu8eq_k130_provenance.
- NP219803.RAUTAD_obKWj2MjSV9GhwSfwX9ciNIi2kuf3U-bu8eq_k130_assertion wasGeneratedBy ECO_0000203 NP219803.RAUTAD_obKWj2MjSV9GhwSfwX9ciNIi2kuf3U-bu8eq_k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP219803.RAUTAD_obKWj2MjSV9GhwSfwX9ciNIi2kuf3U-bu8eq_k130_provenance.