Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP806424.RAMCwTBeUovTTMl5ZEIsN5AXUvyVG2IDyNgfROIEoTXUE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP806424.RAMCwTBeUovTTMl5ZEIsN5AXUvyVG2IDyNgfROIEoTXUE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP806424.RAMCwTBeUovTTMl5ZEIsN5AXUvyVG2IDyNgfROIEoTXUE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP806424.RAMCwTBeUovTTMl5ZEIsN5AXUvyVG2IDyNgfROIEoTXUE130_provenance.
- NP806424.RAMCwTBeUovTTMl5ZEIsN5AXUvyVG2IDyNgfROIEoTXUE130_assertion description "[More recently mutations in the HESX1, the LHX3 and LHX4 transcription factor genes have also been described as a cause in patients with CPHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806424.RAMCwTBeUovTTMl5ZEIsN5AXUvyVG2IDyNgfROIEoTXUE130_provenance.
- NP806424.RAMCwTBeUovTTMl5ZEIsN5AXUvyVG2IDyNgfROIEoTXUE130_assertion evidence source_evidence_literature NP806424.RAMCwTBeUovTTMl5ZEIsN5AXUvyVG2IDyNgfROIEoTXUE130_provenance.
- NP806424.RAMCwTBeUovTTMl5ZEIsN5AXUvyVG2IDyNgfROIEoTXUE130_assertion SIO_000772 12812307 NP806424.RAMCwTBeUovTTMl5ZEIsN5AXUvyVG2IDyNgfROIEoTXUE130_provenance.
- NP806424.RAMCwTBeUovTTMl5ZEIsN5AXUvyVG2IDyNgfROIEoTXUE130_assertion wasDerivedFrom befree-20150227 NP806424.RAMCwTBeUovTTMl5ZEIsN5AXUvyVG2IDyNgfROIEoTXUE130_provenance.
- NP806424.RAMCwTBeUovTTMl5ZEIsN5AXUvyVG2IDyNgfROIEoTXUE130_assertion wasGeneratedBy ECO_0000203 NP806424.RAMCwTBeUovTTMl5ZEIsN5AXUvyVG2IDyNgfROIEoTXUE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP806424.RAMCwTBeUovTTMl5ZEIsN5AXUvyVG2IDyNgfROIEoTXUE130_provenance.