Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP856409.RAQAR2U9SxzA5PMqwAyiYGAKLoVXcXf3oPreDBHNo4W_k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP856409.RAQAR2U9SxzA5PMqwAyiYGAKLoVXcXf3oPreDBHNo4W_k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP856409.RAQAR2U9SxzA5PMqwAyiYGAKLoVXcXf3oPreDBHNo4W_k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP856409.RAQAR2U9SxzA5PMqwAyiYGAKLoVXcXf3oPreDBHNo4W_k130_provenance.
- NP856409.RAQAR2U9SxzA5PMqwAyiYGAKLoVXcXf3oPreDBHNo4W_k130_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." NP856409.RAQAR2U9SxzA5PMqwAyiYGAKLoVXcXf3oPreDBHNo4W_k130_provenance.
- NP856409.RAQAR2U9SxzA5PMqwAyiYGAKLoVXcXf3oPreDBHNo4W_k130_assertion evidence source_evidence_literature NP856409.RAQAR2U9SxzA5PMqwAyiYGAKLoVXcXf3oPreDBHNo4W_k130_provenance.
- NP856409.RAQAR2U9SxzA5PMqwAyiYGAKLoVXcXf3oPreDBHNo4W_k130_assertion SIO_000772 16773131 NP856409.RAQAR2U9SxzA5PMqwAyiYGAKLoVXcXf3oPreDBHNo4W_k130_provenance.
- NP856409.RAQAR2U9SxzA5PMqwAyiYGAKLoVXcXf3oPreDBHNo4W_k130_assertion wasDerivedFrom befree-20140225 NP856409.RAQAR2U9SxzA5PMqwAyiYGAKLoVXcXf3oPreDBHNo4W_k130_provenance.
- NP856409.RAQAR2U9SxzA5PMqwAyiYGAKLoVXcXf3oPreDBHNo4W_k130_assertion wasGeneratedBy ECO_0000203 NP856409.RAQAR2U9SxzA5PMqwAyiYGAKLoVXcXf3oPreDBHNo4W_k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP856409.RAQAR2U9SxzA5PMqwAyiYGAKLoVXcXf3oPreDBHNo4W_k130_provenance.