Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1155243.RAOBsIVUyze587lWdEbaAfzHj0AhwkPi6G7GergGE8OYk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1155243.RAOBsIVUyze587lWdEbaAfzHj0AhwkPi6G7GergGE8OYk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1155243.RAOBsIVUyze587lWdEbaAfzHj0AhwkPi6G7GergGE8OYk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1155243.RAOBsIVUyze587lWdEbaAfzHj0AhwkPi6G7GergGE8OYk130_provenance.
- NP1155243.RAOBsIVUyze587lWdEbaAfzHj0AhwkPi6G7GergGE8OYk130_assertion description "[The c.429_452dup24 of the ARX gene is a rare genetic anomaly, leading to X-Linked Intellectual Disability without brain malformation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1155243.RAOBsIVUyze587lWdEbaAfzHj0AhwkPi6G7GergGE8OYk130_provenance.
- NP1155243.RAOBsIVUyze587lWdEbaAfzHj0AhwkPi6G7GergGE8OYk130_assertion evidence source_evidence_literature NP1155243.RAOBsIVUyze587lWdEbaAfzHj0AhwkPi6G7GergGE8OYk130_provenance.
- NP1155243.RAOBsIVUyze587lWdEbaAfzHj0AhwkPi6G7GergGE8OYk130_assertion SIO_000772 24528893 NP1155243.RAOBsIVUyze587lWdEbaAfzHj0AhwkPi6G7GergGE8OYk130_provenance.
- NP1155243.RAOBsIVUyze587lWdEbaAfzHj0AhwkPi6G7GergGE8OYk130_assertion wasDerivedFrom befree-2016 NP1155243.RAOBsIVUyze587lWdEbaAfzHj0AhwkPi6G7GergGE8OYk130_provenance.
- NP1155243.RAOBsIVUyze587lWdEbaAfzHj0AhwkPi6G7GergGE8OYk130_assertion wasGeneratedBy ECO_0000203 NP1155243.RAOBsIVUyze587lWdEbaAfzHj0AhwkPi6G7GergGE8OYk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1155243.RAOBsIVUyze587lWdEbaAfzHj0AhwkPi6G7GergGE8OYk130_provenance.