Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP420006.RAaRLpVGHhIWdPKBXpVSeT3TtlDgjxp66UkLVmwZgv6xw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP420006.RAaRLpVGHhIWdPKBXpVSeT3TtlDgjxp66UkLVmwZgv6xw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420006.RAaRLpVGHhIWdPKBXpVSeT3TtlDgjxp66UkLVmwZgv6xw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420006.RAaRLpVGHhIWdPKBXpVSeT3TtlDgjxp66UkLVmwZgv6xw130_provenance.
- NP420006.RAaRLpVGHhIWdPKBXpVSeT3TtlDgjxp66UkLVmwZgv6xw130_assertion description "[We conclude that patients with GCPS caused by large deletions that include GLI3 are likely to have cognitive deficits, and we hypothesize that this severe GCPS phenotype is caused by deletion of contiguous genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420006.RAaRLpVGHhIWdPKBXpVSeT3TtlDgjxp66UkLVmwZgv6xw130_provenance.
- NP420006.RAaRLpVGHhIWdPKBXpVSeT3TtlDgjxp66UkLVmwZgv6xw130_assertion evidence source_evidence_literature NP420006.RAaRLpVGHhIWdPKBXpVSeT3TtlDgjxp66UkLVmwZgv6xw130_provenance.
- NP420006.RAaRLpVGHhIWdPKBXpVSeT3TtlDgjxp66UkLVmwZgv6xw130_assertion SIO_000772 14608643 NP420006.RAaRLpVGHhIWdPKBXpVSeT3TtlDgjxp66UkLVmwZgv6xw130_provenance.
- NP420006.RAaRLpVGHhIWdPKBXpVSeT3TtlDgjxp66UkLVmwZgv6xw130_assertion wasDerivedFrom befree-2016 NP420006.RAaRLpVGHhIWdPKBXpVSeT3TtlDgjxp66UkLVmwZgv6xw130_provenance.
- NP420006.RAaRLpVGHhIWdPKBXpVSeT3TtlDgjxp66UkLVmwZgv6xw130_assertion wasGeneratedBy ECO_0000203 NP420006.RAaRLpVGHhIWdPKBXpVSeT3TtlDgjxp66UkLVmwZgv6xw130_provenance.
- befree-2016 importedOn "2016-02-19" NP420006.RAaRLpVGHhIWdPKBXpVSeT3TtlDgjxp66UkLVmwZgv6xw130_provenance.