Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP135078.RANYklYurdQdZ-H3N8nBbtXmmi-Ur5snMZ9dqd2k3FOEo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP135078.RANYklYurdQdZ-H3N8nBbtXmmi-Ur5snMZ9dqd2k3FOEo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP135078.RANYklYurdQdZ-H3N8nBbtXmmi-Ur5snMZ9dqd2k3FOEo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP135078.RANYklYurdQdZ-H3N8nBbtXmmi-Ur5snMZ9dqd2k3FOEo130_provenance.
- NP135078.RANYklYurdQdZ-H3N8nBbtXmmi-Ur5snMZ9dqd2k3FOEo130_assertion wasGeneratedBy ECO_0000203 NP135078.RANYklYurdQdZ-H3N8nBbtXmmi-Ur5snMZ9dqd2k3FOEo130_provenance.
- NP135078.RANYklYurdQdZ-H3N8nBbtXmmi-Ur5snMZ9dqd2k3FOEo130_assertion wasDerivedFrom lhgdn-20090331 NP135078.RANYklYurdQdZ-H3N8nBbtXmmi-Ur5snMZ9dqd2k3FOEo130_provenance.
- NP135078.RANYklYurdQdZ-H3N8nBbtXmmi-Ur5snMZ9dqd2k3FOEo130_assertion SIO_000772 12724528 NP135078.RANYklYurdQdZ-H3N8nBbtXmmi-Ur5snMZ9dqd2k3FOEo130_provenance.
- NP135078.RANYklYurdQdZ-H3N8nBbtXmmi-Ur5snMZ9dqd2k3FOEo130_assertion evidence source_evidence_literature NP135078.RANYklYurdQdZ-H3N8nBbtXmmi-Ur5snMZ9dqd2k3FOEo130_provenance.
- NP135078.RANYklYurdQdZ-H3N8nBbtXmmi-Ur5snMZ9dqd2k3FOEo130_assertion description "[Mutation of this protein is a risk factor for liver disease of multiple etiologies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135078.RANYklYurdQdZ-H3N8nBbtXmmi-Ur5snMZ9dqd2k3FOEo130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP135078.RANYklYurdQdZ-H3N8nBbtXmmi-Ur5snMZ9dqd2k3FOEo130_provenance.