Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP276034.RAL8szXjHWKbFpY9EhViiUpVN985WzHPajFM5yiOenBIU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP276034.RAL8szXjHWKbFpY9EhViiUpVN985WzHPajFM5yiOenBIU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP276034.RAL8szXjHWKbFpY9EhViiUpVN985WzHPajFM5yiOenBIU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP276034.RAL8szXjHWKbFpY9EhViiUpVN985WzHPajFM5yiOenBIU130_provenance.
- NP276034.RAL8szXjHWKbFpY9EhViiUpVN985WzHPajFM5yiOenBIU130_assertion description "[PITX2 mutations are known to be responsible for Axenfield Rieger syndrome, a genetic disorder in which pituitary abnormalities have been detected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276034.RAL8szXjHWKbFpY9EhViiUpVN985WzHPajFM5yiOenBIU130_provenance.
- NP276034.RAL8szXjHWKbFpY9EhViiUpVN985WzHPajFM5yiOenBIU130_assertion evidence source_evidence_literature NP276034.RAL8szXjHWKbFpY9EhViiUpVN985WzHPajFM5yiOenBIU130_provenance.
- NP276034.RAL8szXjHWKbFpY9EhViiUpVN985WzHPajFM5yiOenBIU130_assertion SIO_000772 21810944 NP276034.RAL8szXjHWKbFpY9EhViiUpVN985WzHPajFM5yiOenBIU130_provenance.
- NP276034.RAL8szXjHWKbFpY9EhViiUpVN985WzHPajFM5yiOenBIU130_assertion wasDerivedFrom befree-20140225 NP276034.RAL8szXjHWKbFpY9EhViiUpVN985WzHPajFM5yiOenBIU130_provenance.
- NP276034.RAL8szXjHWKbFpY9EhViiUpVN985WzHPajFM5yiOenBIU130_assertion wasGeneratedBy ECO_0000203 NP276034.RAL8szXjHWKbFpY9EhViiUpVN985WzHPajFM5yiOenBIU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP276034.RAL8szXjHWKbFpY9EhViiUpVN985WzHPajFM5yiOenBIU130_provenance.