Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP449489.RAatwI-vIGtf6MAiL_MLt4yGglc9Mb6HQ8ToWqwvF4G_w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP449489.RAatwI-vIGtf6MAiL_MLt4yGglc9Mb6HQ8ToWqwvF4G_w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP449489.RAatwI-vIGtf6MAiL_MLt4yGglc9Mb6HQ8ToWqwvF4G_w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP449489.RAatwI-vIGtf6MAiL_MLt4yGglc9Mb6HQ8ToWqwvF4G_w130_provenance.
- NP449489.RAatwI-vIGtf6MAiL_MLt4yGglc9Mb6HQ8ToWqwvF4G_w130_assertion description "[In addition to craniosynostosis with crouzonoid facies and acanthosis nigricans (present in all patients), melanocytic nevi, choanal atresia or stenosis, hydrocephalus, Chiari malformations and oral abnormalities were observed in the majority of the 35 patients analyzed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP449489.RAatwI-vIGtf6MAiL_MLt4yGglc9Mb6HQ8ToWqwvF4G_w130_provenance.
- NP449489.RAatwI-vIGtf6MAiL_MLt4yGglc9Mb6HQ8ToWqwvF4G_w130_assertion evidence source_evidence_literature NP449489.RAatwI-vIGtf6MAiL_MLt4yGglc9Mb6HQ8ToWqwvF4G_w130_provenance.
- NP449489.RAatwI-vIGtf6MAiL_MLt4yGglc9Mb6HQ8ToWqwvF4G_w130_assertion SIO_000772 17935505 NP449489.RAatwI-vIGtf6MAiL_MLt4yGglc9Mb6HQ8ToWqwvF4G_w130_provenance.
- NP449489.RAatwI-vIGtf6MAiL_MLt4yGglc9Mb6HQ8ToWqwvF4G_w130_assertion wasDerivedFrom befree-20140225 NP449489.RAatwI-vIGtf6MAiL_MLt4yGglc9Mb6HQ8ToWqwvF4G_w130_provenance.
- NP449489.RAatwI-vIGtf6MAiL_MLt4yGglc9Mb6HQ8ToWqwvF4G_w130_assertion wasGeneratedBy ECO_0000203 NP449489.RAatwI-vIGtf6MAiL_MLt4yGglc9Mb6HQ8ToWqwvF4G_w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP449489.RAatwI-vIGtf6MAiL_MLt4yGglc9Mb6HQ8ToWqwvF4G_w130_provenance.