Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP146567.RAvR-JCImNAI8UjGiB5-bynPKwpNxE6rj8aGo21B6R0fQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP146567.RAvR-JCImNAI8UjGiB5-bynPKwpNxE6rj8aGo21B6R0fQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP146567.RAvR-JCImNAI8UjGiB5-bynPKwpNxE6rj8aGo21B6R0fQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP146567.RAvR-JCImNAI8UjGiB5-bynPKwpNxE6rj8aGo21B6R0fQ130_provenance.
- NP146567.RAvR-JCImNAI8UjGiB5-bynPKwpNxE6rj8aGo21B6R0fQ130_assertion description "[ZFHX1B may be an important gene for normal embryonic neural crest development/indicate that Hirschsprung's disease can be regarded as a congenital malformation/were located at exon 8 of ZFHX1B in 3 of 4 cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146567.RAvR-JCImNAI8UjGiB5-bynPKwpNxE6rj8aGo21B6R0fQ130_provenance.
- NP146567.RAvR-JCImNAI8UjGiB5-bynPKwpNxE6rj8aGo21B6R0fQ130_assertion evidence source_evidence_literature NP146567.RAvR-JCImNAI8UjGiB5-bynPKwpNxE6rj8aGo21B6R0fQ130_provenance.
- NP146567.RAvR-JCImNAI8UjGiB5-bynPKwpNxE6rj8aGo21B6R0fQ130_assertion SIO_000772 12149685 NP146567.RAvR-JCImNAI8UjGiB5-bynPKwpNxE6rj8aGo21B6R0fQ130_provenance.
- NP146567.RAvR-JCImNAI8UjGiB5-bynPKwpNxE6rj8aGo21B6R0fQ130_assertion wasDerivedFrom lhgdn-20090331 NP146567.RAvR-JCImNAI8UjGiB5-bynPKwpNxE6rj8aGo21B6R0fQ130_provenance.
- NP146567.RAvR-JCImNAI8UjGiB5-bynPKwpNxE6rj8aGo21B6R0fQ130_assertion wasGeneratedBy ECO_0000203 NP146567.RAvR-JCImNAI8UjGiB5-bynPKwpNxE6rj8aGo21B6R0fQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP146567.RAvR-JCImNAI8UjGiB5-bynPKwpNxE6rj8aGo21B6R0fQ130_provenance.