Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP196853.RA2DIve4QNM3cPuxZUXHq2Fxnf3KRLhAuIUDm-pq9Z6QU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP196853.RA2DIve4QNM3cPuxZUXHq2Fxnf3KRLhAuIUDm-pq9Z6QU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP196853.RA2DIve4QNM3cPuxZUXHq2Fxnf3KRLhAuIUDm-pq9Z6QU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP196853.RA2DIve4QNM3cPuxZUXHq2Fxnf3KRLhAuIUDm-pq9Z6QU130_provenance.
- NP196853.RA2DIve4QNM3cPuxZUXHq2Fxnf3KRLhAuIUDm-pq9Z6QU130_assertion description "[Inter- and intrafamilial variability is a well-known feature of the L1CAM spectrum, and several patients have a combination of L1CAM mutations and Hirschsprung's disease (HSCR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP196853.RA2DIve4QNM3cPuxZUXHq2Fxnf3KRLhAuIUDm-pq9Z6QU130_provenance.
- NP196853.RA2DIve4QNM3cPuxZUXHq2Fxnf3KRLhAuIUDm-pq9Z6QU130_assertion evidence source_evidence_literature NP196853.RA2DIve4QNM3cPuxZUXHq2Fxnf3KRLhAuIUDm-pq9Z6QU130_provenance.
- NP196853.RA2DIve4QNM3cPuxZUXHq2Fxnf3KRLhAuIUDm-pq9Z6QU130_assertion SIO_000772 16650080 NP196853.RA2DIve4QNM3cPuxZUXHq2Fxnf3KRLhAuIUDm-pq9Z6QU130_provenance.
- NP196853.RA2DIve4QNM3cPuxZUXHq2Fxnf3KRLhAuIUDm-pq9Z6QU130_assertion wasDerivedFrom befree-20140225 NP196853.RA2DIve4QNM3cPuxZUXHq2Fxnf3KRLhAuIUDm-pq9Z6QU130_provenance.
- NP196853.RA2DIve4QNM3cPuxZUXHq2Fxnf3KRLhAuIUDm-pq9Z6QU130_assertion wasGeneratedBy ECO_0000203 NP196853.RA2DIve4QNM3cPuxZUXHq2Fxnf3KRLhAuIUDm-pq9Z6QU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP196853.RA2DIve4QNM3cPuxZUXHq2Fxnf3KRLhAuIUDm-pq9Z6QU130_provenance.