Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP922006.RALYiB3rkGRNbKZdPo2kOAgPHajkWSstaVWVjIOKjJqdo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP922006.RALYiB3rkGRNbKZdPo2kOAgPHajkWSstaVWVjIOKjJqdo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP922006.RALYiB3rkGRNbKZdPo2kOAgPHajkWSstaVWVjIOKjJqdo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP922006.RALYiB3rkGRNbKZdPo2kOAgPHajkWSstaVWVjIOKjJqdo130_provenance.
- NP922006.RALYiB3rkGRNbKZdPo2kOAgPHajkWSstaVWVjIOKjJqdo130_assertion description "[ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP922006.RALYiB3rkGRNbKZdPo2kOAgPHajkWSstaVWVjIOKjJqdo130_provenance.
- NP922006.RALYiB3rkGRNbKZdPo2kOAgPHajkWSstaVWVjIOKjJqdo130_assertion evidence source_evidence_literature NP922006.RALYiB3rkGRNbKZdPo2kOAgPHajkWSstaVWVjIOKjJqdo130_provenance.
- NP922006.RALYiB3rkGRNbKZdPo2kOAgPHajkWSstaVWVjIOKjJqdo130_assertion SIO_000772 23623388 NP922006.RALYiB3rkGRNbKZdPo2kOAgPHajkWSstaVWVjIOKjJqdo130_provenance.
- NP922006.RALYiB3rkGRNbKZdPo2kOAgPHajkWSstaVWVjIOKjJqdo130_assertion wasDerivedFrom befree-20150227 NP922006.RALYiB3rkGRNbKZdPo2kOAgPHajkWSstaVWVjIOKjJqdo130_provenance.
- NP922006.RALYiB3rkGRNbKZdPo2kOAgPHajkWSstaVWVjIOKjJqdo130_assertion wasGeneratedBy ECO_0000203 NP922006.RALYiB3rkGRNbKZdPo2kOAgPHajkWSstaVWVjIOKjJqdo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP922006.RALYiB3rkGRNbKZdPo2kOAgPHajkWSstaVWVjIOKjJqdo130_provenance.