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- source_evidence_literature type ECO_0000212 NP835533.RAK-U36rm5UO77EFCaK7jwmsq-2kbmo3TvEIFAJnee5zY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP835533.RAK-U36rm5UO77EFCaK7jwmsq-2kbmo3TvEIFAJnee5zY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP835533.RAK-U36rm5UO77EFCaK7jwmsq-2kbmo3TvEIFAJnee5zY130_provenance.
- NP835533.RAK-U36rm5UO77EFCaK7jwmsq-2kbmo3TvEIFAJnee5zY130_assertion description "[The authors report detailed clinical and developmental assessment of 3 brothers who were found to carry a novel mutation in the ARX gene associated with a relatively mild phenotype of static global developmental delay and early hand preference.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835533.RAK-U36rm5UO77EFCaK7jwmsq-2kbmo3TvEIFAJnee5zY130_provenance.
- NP835533.RAK-U36rm5UO77EFCaK7jwmsq-2kbmo3TvEIFAJnee5zY130_assertion evidence source_evidence_literature NP835533.RAK-U36rm5UO77EFCaK7jwmsq-2kbmo3TvEIFAJnee5zY130_provenance.
- NP835533.RAK-U36rm5UO77EFCaK7jwmsq-2kbmo3TvEIFAJnee5zY130_assertion SIO_000772 22922607 NP835533.RAK-U36rm5UO77EFCaK7jwmsq-2kbmo3TvEIFAJnee5zY130_provenance.
- NP835533.RAK-U36rm5UO77EFCaK7jwmsq-2kbmo3TvEIFAJnee5zY130_assertion wasDerivedFrom befree-20150227 NP835533.RAK-U36rm5UO77EFCaK7jwmsq-2kbmo3TvEIFAJnee5zY130_provenance.
- NP835533.RAK-U36rm5UO77EFCaK7jwmsq-2kbmo3TvEIFAJnee5zY130_assertion wasGeneratedBy ECO_0000203 NP835533.RAK-U36rm5UO77EFCaK7jwmsq-2kbmo3TvEIFAJnee5zY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP835533.RAK-U36rm5UO77EFCaK7jwmsq-2kbmo3TvEIFAJnee5zY130_provenance.