Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP498599.RAwMTPPxPSxhxdSbtWIve_22aZJaHuS8sn2t34UXqHdP0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP498599.RAwMTPPxPSxhxdSbtWIve_22aZJaHuS8sn2t34UXqHdP0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP498599.RAwMTPPxPSxhxdSbtWIve_22aZJaHuS8sn2t34UXqHdP0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP498599.RAwMTPPxPSxhxdSbtWIve_22aZJaHuS8sn2t34UXqHdP0130_provenance.
- NP498599.RAwMTPPxPSxhxdSbtWIve_22aZJaHuS8sn2t34UXqHdP0130_assertion description "[Chromosome 22 tiling-path array-CGH analysis identifies germ-line- and tumor-specific aberrations in patients with glioblastoma multiforme.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP498599.RAwMTPPxPSxhxdSbtWIve_22aZJaHuS8sn2t34UXqHdP0130_provenance.
- NP498599.RAwMTPPxPSxhxdSbtWIve_22aZJaHuS8sn2t34UXqHdP0130_assertion evidence source_evidence_literature NP498599.RAwMTPPxPSxhxdSbtWIve_22aZJaHuS8sn2t34UXqHdP0130_provenance.
- NP498599.RAwMTPPxPSxhxdSbtWIve_22aZJaHuS8sn2t34UXqHdP0130_assertion SIO_000772 15945096 NP498599.RAwMTPPxPSxhxdSbtWIve_22aZJaHuS8sn2t34UXqHdP0130_provenance.
- NP498599.RAwMTPPxPSxhxdSbtWIve_22aZJaHuS8sn2t34UXqHdP0130_assertion wasDerivedFrom befree-2016 NP498599.RAwMTPPxPSxhxdSbtWIve_22aZJaHuS8sn2t34UXqHdP0130_provenance.
- NP498599.RAwMTPPxPSxhxdSbtWIve_22aZJaHuS8sn2t34UXqHdP0130_assertion wasGeneratedBy ECO_0000203 NP498599.RAwMTPPxPSxhxdSbtWIve_22aZJaHuS8sn2t34UXqHdP0130_provenance.
- befree-2016 importedOn "2016-02-19" NP498599.RAwMTPPxPSxhxdSbtWIve_22aZJaHuS8sn2t34UXqHdP0130_provenance.