Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP262484.RAwecuZDgTAttPguyXGv9ZNFuqD2V3ZNy8Hzt2Fu5wUmc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP262484.RAwecuZDgTAttPguyXGv9ZNFuqD2V3ZNy8Hzt2Fu5wUmc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP262484.RAwecuZDgTAttPguyXGv9ZNFuqD2V3ZNy8Hzt2Fu5wUmc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP262484.RAwecuZDgTAttPguyXGv9ZNFuqD2V3ZNy8Hzt2Fu5wUmc130_provenance.
- NP262484.RAwecuZDgTAttPguyXGv9ZNFuqD2V3ZNy8Hzt2Fu5wUmc130_assertion description "[All NB susceptibility genes replicated in the Italian dataset except for DDX4 and IL31RA, and the most significant SNP was rs6435862 in BARD1 (P = 8.4 � 10(-15)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262484.RAwecuZDgTAttPguyXGv9ZNFuqD2V3ZNy8Hzt2Fu5wUmc130_provenance.
- NP262484.RAwecuZDgTAttPguyXGv9ZNFuqD2V3ZNy8Hzt2Fu5wUmc130_assertion evidence source_evidence_literature NP262484.RAwecuZDgTAttPguyXGv9ZNFuqD2V3ZNy8Hzt2Fu5wUmc130_provenance.
- NP262484.RAwecuZDgTAttPguyXGv9ZNFuqD2V3ZNy8Hzt2Fu5wUmc130_assertion SIO_000772 23222812 NP262484.RAwecuZDgTAttPguyXGv9ZNFuqD2V3ZNy8Hzt2Fu5wUmc130_provenance.
- NP262484.RAwecuZDgTAttPguyXGv9ZNFuqD2V3ZNy8Hzt2Fu5wUmc130_assertion wasDerivedFrom befree-20140225 NP262484.RAwecuZDgTAttPguyXGv9ZNFuqD2V3ZNy8Hzt2Fu5wUmc130_provenance.
- NP262484.RAwecuZDgTAttPguyXGv9ZNFuqD2V3ZNy8Hzt2Fu5wUmc130_assertion wasGeneratedBy ECO_0000203 NP262484.RAwecuZDgTAttPguyXGv9ZNFuqD2V3ZNy8Hzt2Fu5wUmc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP262484.RAwecuZDgTAttPguyXGv9ZNFuqD2V3ZNy8Hzt2Fu5wUmc130_provenance.