Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP275333.RAmC1zwxc06EK6eGXGwQv4aBmWevlYAggtuwtm4hlHg3Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP275333.RAmC1zwxc06EK6eGXGwQv4aBmWevlYAggtuwtm4hlHg3Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP275333.RAmC1zwxc06EK6eGXGwQv4aBmWevlYAggtuwtm4hlHg3Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP275333.RAmC1zwxc06EK6eGXGwQv4aBmWevlYAggtuwtm4hlHg3Q130_provenance.
- NP275333.RAmC1zwxc06EK6eGXGwQv4aBmWevlYAggtuwtm4hlHg3Q130_assertion description "[A history of digital anomalies in the father and grandfather lead to the diagnosis of dominantly inherited Greig cephalopolysyndactyly syndrome (GCPS, MIM #175700).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP275333.RAmC1zwxc06EK6eGXGwQv4aBmWevlYAggtuwtm4hlHg3Q130_provenance.
- NP275333.RAmC1zwxc06EK6eGXGwQv4aBmWevlYAggtuwtm4hlHg3Q130_assertion evidence source_evidence_literature NP275333.RAmC1zwxc06EK6eGXGwQv4aBmWevlYAggtuwtm4hlHg3Q130_provenance.
- NP275333.RAmC1zwxc06EK6eGXGwQv4aBmWevlYAggtuwtm4hlHg3Q130_assertion SIO_000772 10678662 NP275333.RAmC1zwxc06EK6eGXGwQv4aBmWevlYAggtuwtm4hlHg3Q130_provenance.
- NP275333.RAmC1zwxc06EK6eGXGwQv4aBmWevlYAggtuwtm4hlHg3Q130_assertion wasDerivedFrom befree-2016 NP275333.RAmC1zwxc06EK6eGXGwQv4aBmWevlYAggtuwtm4hlHg3Q130_provenance.
- NP275333.RAmC1zwxc06EK6eGXGwQv4aBmWevlYAggtuwtm4hlHg3Q130_assertion wasGeneratedBy ECO_0000203 NP275333.RAmC1zwxc06EK6eGXGwQv4aBmWevlYAggtuwtm4hlHg3Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP275333.RAmC1zwxc06EK6eGXGwQv4aBmWevlYAggtuwtm4hlHg3Q130_provenance.