Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_provenance.
- NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_assertion description "[X-linked isolated lissencephaly sequence (ILS) and subcortical band heterotopia are allelic human disorders associated with mutations of the DCX gene in both familial and sporadic forms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_provenance.
- NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_assertion evidence source_evidence_literature NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_provenance.
- NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_assertion SIO_000772 11468322 NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_provenance.
- NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_assertion wasDerivedFrom befree-2016 NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_provenance.
- NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_assertion wasGeneratedBy ECO_0000203 NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_provenance.