Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_provenance.
- NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_assertion description "[We first screened 153 patients with MR and facial dysmorphism associated with malformations, or growth anomalies, or familial history, with cytogenetically normal chromosomes, and the absence of FRAXA mutation and subtelomeric rearrangements.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_provenance.
- NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_assertion evidence source_evidence_literature NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_provenance.
- NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_assertion SIO_000772 16773131 NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_provenance.
- NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_assertion wasDerivedFrom befree-2016 NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_provenance.
- NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_assertion wasGeneratedBy ECO_0000203 NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_provenance.
- befree-2016 importedOn "2016-02-19" NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_provenance.