Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP344654.RAnnVAAGytim3dREj1JIJYZmGXsKAxJZ9OqHAuB1NyChk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP344654.RAnnVAAGytim3dREj1JIJYZmGXsKAxJZ9OqHAuB1NyChk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP344654.RAnnVAAGytim3dREj1JIJYZmGXsKAxJZ9OqHAuB1NyChk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP344654.RAnnVAAGytim3dREj1JIJYZmGXsKAxJZ9OqHAuB1NyChk130_provenance.
- NP344654.RAnnVAAGytim3dREj1JIJYZmGXsKAxJZ9OqHAuB1NyChk130_assertion description "[FATP4 mutations in humans cause ichthyosis prematurity syndrome (IPS), and mutations of Fatp4 in mice have previously been found to cause a phenotype that resembles human congenital ichthyoses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP344654.RAnnVAAGytim3dREj1JIJYZmGXsKAxJZ9OqHAuB1NyChk130_provenance.
- NP344654.RAnnVAAGytim3dREj1JIJYZmGXsKAxJZ9OqHAuB1NyChk130_assertion evidence source_evidence_literature NP344654.RAnnVAAGytim3dREj1JIJYZmGXsKAxJZ9OqHAuB1NyChk130_provenance.
- NP344654.RAnnVAAGytim3dREj1JIJYZmGXsKAxJZ9OqHAuB1NyChk130_assertion SIO_000772 23226340 NP344654.RAnnVAAGytim3dREj1JIJYZmGXsKAxJZ9OqHAuB1NyChk130_provenance.
- NP344654.RAnnVAAGytim3dREj1JIJYZmGXsKAxJZ9OqHAuB1NyChk130_assertion wasDerivedFrom befree-20140225 NP344654.RAnnVAAGytim3dREj1JIJYZmGXsKAxJZ9OqHAuB1NyChk130_provenance.
- NP344654.RAnnVAAGytim3dREj1JIJYZmGXsKAxJZ9OqHAuB1NyChk130_assertion wasGeneratedBy ECO_0000203 NP344654.RAnnVAAGytim3dREj1JIJYZmGXsKAxJZ9OqHAuB1NyChk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP344654.RAnnVAAGytim3dREj1JIJYZmGXsKAxJZ9OqHAuB1NyChk130_provenance.