Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP376509.RA25_eH-B9nYxDu8zF4L0uBJd2I3zhirClrPeve4qVscY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP376509.RA25_eH-B9nYxDu8zF4L0uBJd2I3zhirClrPeve4qVscY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP376509.RA25_eH-B9nYxDu8zF4L0uBJd2I3zhirClrPeve4qVscY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP376509.RA25_eH-B9nYxDu8zF4L0uBJd2I3zhirClrPeve4qVscY130_provenance.
- NP376509.RA25_eH-B9nYxDu8zF4L0uBJd2I3zhirClrPeve4qVscY130_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." NP376509.RA25_eH-B9nYxDu8zF4L0uBJd2I3zhirClrPeve4qVscY130_provenance.
- NP376509.RA25_eH-B9nYxDu8zF4L0uBJd2I3zhirClrPeve4qVscY130_assertion evidence source_evidence_literature NP376509.RA25_eH-B9nYxDu8zF4L0uBJd2I3zhirClrPeve4qVscY130_provenance.
- NP376509.RA25_eH-B9nYxDu8zF4L0uBJd2I3zhirClrPeve4qVscY130_assertion SIO_000772 12812307 NP376509.RA25_eH-B9nYxDu8zF4L0uBJd2I3zhirClrPeve4qVscY130_provenance.
- NP376509.RA25_eH-B9nYxDu8zF4L0uBJd2I3zhirClrPeve4qVscY130_assertion wasDerivedFrom befree-20140225 NP376509.RA25_eH-B9nYxDu8zF4L0uBJd2I3zhirClrPeve4qVscY130_provenance.
- NP376509.RA25_eH-B9nYxDu8zF4L0uBJd2I3zhirClrPeve4qVscY130_assertion wasGeneratedBy ECO_0000203 NP376509.RA25_eH-B9nYxDu8zF4L0uBJd2I3zhirClrPeve4qVscY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP376509.RA25_eH-B9nYxDu8zF4L0uBJd2I3zhirClrPeve4qVscY130_provenance.