Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP729177.RA438JN_PUFdtc323IdkCGzqh67H2DckN-vqgfIcmR_vc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP729177.RA438JN_PUFdtc323IdkCGzqh67H2DckN-vqgfIcmR_vc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP729177.RA438JN_PUFdtc323IdkCGzqh67H2DckN-vqgfIcmR_vc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP729177.RA438JN_PUFdtc323IdkCGzqh67H2DckN-vqgfIcmR_vc130_provenance.
- NP729177.RA438JN_PUFdtc323IdkCGzqh67H2DckN-vqgfIcmR_vc130_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." NP729177.RA438JN_PUFdtc323IdkCGzqh67H2DckN-vqgfIcmR_vc130_provenance.
- NP729177.RA438JN_PUFdtc323IdkCGzqh67H2DckN-vqgfIcmR_vc130_assertion evidence source_evidence_literature NP729177.RA438JN_PUFdtc323IdkCGzqh67H2DckN-vqgfIcmR_vc130_provenance.
- NP729177.RA438JN_PUFdtc323IdkCGzqh67H2DckN-vqgfIcmR_vc130_assertion SIO_000772 23623388 NP729177.RA438JN_PUFdtc323IdkCGzqh67H2DckN-vqgfIcmR_vc130_provenance.
- NP729177.RA438JN_PUFdtc323IdkCGzqh67H2DckN-vqgfIcmR_vc130_assertion wasDerivedFrom befree-20140225 NP729177.RA438JN_PUFdtc323IdkCGzqh67H2DckN-vqgfIcmR_vc130_provenance.
- NP729177.RA438JN_PUFdtc323IdkCGzqh67H2DckN-vqgfIcmR_vc130_assertion wasGeneratedBy ECO_0000203 NP729177.RA438JN_PUFdtc323IdkCGzqh67H2DckN-vqgfIcmR_vc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP729177.RA438JN_PUFdtc323IdkCGzqh67H2DckN-vqgfIcmR_vc130_provenance.