Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1044169.RAdPYJiufLJNzs2ygI52qjzSvh7umbE7i4w4h0pDmpMXw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1044169.RAdPYJiufLJNzs2ygI52qjzSvh7umbE7i4w4h0pDmpMXw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1044169.RAdPYJiufLJNzs2ygI52qjzSvh7umbE7i4w4h0pDmpMXw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1044169.RAdPYJiufLJNzs2ygI52qjzSvh7umbE7i4w4h0pDmpMXw130_provenance.
- NP1044169.RAdPYJiufLJNzs2ygI52qjzSvh7umbE7i4w4h0pDmpMXw130_assertion description "[Rare missense neuronal cadherin gene (CDH2) variants in specific obsessive-compulsive disorder and Tourette disorder phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1044169.RAdPYJiufLJNzs2ygI52qjzSvh7umbE7i4w4h0pDmpMXw130_provenance.
- NP1044169.RAdPYJiufLJNzs2ygI52qjzSvh7umbE7i4w4h0pDmpMXw130_assertion evidence source_evidence_literature NP1044169.RAdPYJiufLJNzs2ygI52qjzSvh7umbE7i4w4h0pDmpMXw130_provenance.
- NP1044169.RAdPYJiufLJNzs2ygI52qjzSvh7umbE7i4w4h0pDmpMXw130_assertion SIO_000772 23321619 NP1044169.RAdPYJiufLJNzs2ygI52qjzSvh7umbE7i4w4h0pDmpMXw130_provenance.
- NP1044169.RAdPYJiufLJNzs2ygI52qjzSvh7umbE7i4w4h0pDmpMXw130_assertion wasDerivedFrom befree-2016 NP1044169.RAdPYJiufLJNzs2ygI52qjzSvh7umbE7i4w4h0pDmpMXw130_provenance.
- NP1044169.RAdPYJiufLJNzs2ygI52qjzSvh7umbE7i4w4h0pDmpMXw130_assertion wasGeneratedBy ECO_0000203 NP1044169.RAdPYJiufLJNzs2ygI52qjzSvh7umbE7i4w4h0pDmpMXw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1044169.RAdPYJiufLJNzs2ygI52qjzSvh7umbE7i4w4h0pDmpMXw130_provenance.