Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP364288.RAfEQUgRHl7jttfRhnK2bT2vAf7Eol1QEMMKHh4lECfNg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP364288.RAfEQUgRHl7jttfRhnK2bT2vAf7Eol1QEMMKHh4lECfNg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP364288.RAfEQUgRHl7jttfRhnK2bT2vAf7Eol1QEMMKHh4lECfNg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP364288.RAfEQUgRHl7jttfRhnK2bT2vAf7Eol1QEMMKHh4lECfNg130_provenance.
- NP364288.RAfEQUgRHl7jttfRhnK2bT2vAf7Eol1QEMMKHh4lECfNg130_assertion description "[Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP364288.RAfEQUgRHl7jttfRhnK2bT2vAf7Eol1QEMMKHh4lECfNg130_provenance.
- NP364288.RAfEQUgRHl7jttfRhnK2bT2vAf7Eol1QEMMKHh4lECfNg130_assertion evidence source_evidence_literature NP364288.RAfEQUgRHl7jttfRhnK2bT2vAf7Eol1QEMMKHh4lECfNg130_provenance.
- NP364288.RAfEQUgRHl7jttfRhnK2bT2vAf7Eol1QEMMKHh4lECfNg130_assertion SIO_000772 17941886 NP364288.RAfEQUgRHl7jttfRhnK2bT2vAf7Eol1QEMMKHh4lECfNg130_provenance.
- NP364288.RAfEQUgRHl7jttfRhnK2bT2vAf7Eol1QEMMKHh4lECfNg130_assertion wasDerivedFrom befree-20150227 NP364288.RAfEQUgRHl7jttfRhnK2bT2vAf7Eol1QEMMKHh4lECfNg130_provenance.
- NP364288.RAfEQUgRHl7jttfRhnK2bT2vAf7Eol1QEMMKHh4lECfNg130_assertion wasGeneratedBy ECO_0000203 NP364288.RAfEQUgRHl7jttfRhnK2bT2vAf7Eol1QEMMKHh4lECfNg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP364288.RAfEQUgRHl7jttfRhnK2bT2vAf7Eol1QEMMKHh4lECfNg130_provenance.