Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP615664.RA6NJG5S7TAJQaUGbpq6qX1Vm0quFw38WgqO4oHUbXTXU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615664.RA6NJG5S7TAJQaUGbpq6qX1Vm0quFw38WgqO4oHUbXTXU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615664.RA6NJG5S7TAJQaUGbpq6qX1Vm0quFw38WgqO4oHUbXTXU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615664.RA6NJG5S7TAJQaUGbpq6qX1Vm0quFw38WgqO4oHUbXTXU130_provenance.
- NP615664.RA6NJG5S7TAJQaUGbpq6qX1Vm0quFw38WgqO4oHUbXTXU130_assertion description "[GPR56 is an orphan G protein - coupled receptor, mutations of which have recently been associated with bilateral frontoparietal polymicrogyria, a rare neurologic disease that has implications in brain development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615664.RA6NJG5S7TAJQaUGbpq6qX1Vm0quFw38WgqO4oHUbXTXU130_provenance.
- NP615664.RA6NJG5S7TAJQaUGbpq6qX1Vm0quFw38WgqO4oHUbXTXU130_assertion evidence source_evidence_literature NP615664.RA6NJG5S7TAJQaUGbpq6qX1Vm0quFw38WgqO4oHUbXTXU130_provenance.
- NP615664.RA6NJG5S7TAJQaUGbpq6qX1Vm0quFw38WgqO4oHUbXTXU130_assertion SIO_000772 17575113 NP615664.RA6NJG5S7TAJQaUGbpq6qX1Vm0quFw38WgqO4oHUbXTXU130_provenance.
- NP615664.RA6NJG5S7TAJQaUGbpq6qX1Vm0quFw38WgqO4oHUbXTXU130_assertion wasDerivedFrom befree-2016 NP615664.RA6NJG5S7TAJQaUGbpq6qX1Vm0quFw38WgqO4oHUbXTXU130_provenance.
- NP615664.RA6NJG5S7TAJQaUGbpq6qX1Vm0quFw38WgqO4oHUbXTXU130_assertion wasGeneratedBy ECO_0000203 NP615664.RA6NJG5S7TAJQaUGbpq6qX1Vm0quFw38WgqO4oHUbXTXU130_provenance.
- befree-2016 importedOn "2016-02-19" NP615664.RA6NJG5S7TAJQaUGbpq6qX1Vm0quFw38WgqO4oHUbXTXU130_provenance.