Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP786836.RADKPHLmVbWKWLLE3YSuA-vdOhsTY99KSM0o7GQgzFGco130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP786836.RADKPHLmVbWKWLLE3YSuA-vdOhsTY99KSM0o7GQgzFGco130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP786836.RADKPHLmVbWKWLLE3YSuA-vdOhsTY99KSM0o7GQgzFGco130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP786836.RADKPHLmVbWKWLLE3YSuA-vdOhsTY99KSM0o7GQgzFGco130_provenance.
- NP786836.RADKPHLmVbWKWLLE3YSuA-vdOhsTY99KSM0o7GQgzFGco130_assertion description "[Here, we describe the positional cloning of SCAMP5, CLIC4 and PPCDC as candidate genes for autism, starting from a person with idiopathic, sporadic autism carrying a de novo chromosomal translocation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP786836.RADKPHLmVbWKWLLE3YSuA-vdOhsTY99KSM0o7GQgzFGco130_provenance.
- NP786836.RADKPHLmVbWKWLLE3YSuA-vdOhsTY99KSM0o7GQgzFGco130_assertion evidence source_evidence_literature NP786836.RADKPHLmVbWKWLLE3YSuA-vdOhsTY99KSM0o7GQgzFGco130_provenance.
- NP786836.RADKPHLmVbWKWLLE3YSuA-vdOhsTY99KSM0o7GQgzFGco130_assertion SIO_000772 20071347 NP786836.RADKPHLmVbWKWLLE3YSuA-vdOhsTY99KSM0o7GQgzFGco130_provenance.
- NP786836.RADKPHLmVbWKWLLE3YSuA-vdOhsTY99KSM0o7GQgzFGco130_assertion wasDerivedFrom befree-2016 NP786836.RADKPHLmVbWKWLLE3YSuA-vdOhsTY99KSM0o7GQgzFGco130_provenance.
- NP786836.RADKPHLmVbWKWLLE3YSuA-vdOhsTY99KSM0o7GQgzFGco130_assertion wasGeneratedBy ECO_0000203 NP786836.RADKPHLmVbWKWLLE3YSuA-vdOhsTY99KSM0o7GQgzFGco130_provenance.
- befree-2016 importedOn "2016-02-19" NP786836.RADKPHLmVbWKWLLE3YSuA-vdOhsTY99KSM0o7GQgzFGco130_provenance.