Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP371019.RAxIwKSUM_xhV1tXZLfkmwcBzSaG6rwlQp8H7bSf5AN5o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP371019.RAxIwKSUM_xhV1tXZLfkmwcBzSaG6rwlQp8H7bSf5AN5o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP371019.RAxIwKSUM_xhV1tXZLfkmwcBzSaG6rwlQp8H7bSf5AN5o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP371019.RAxIwKSUM_xhV1tXZLfkmwcBzSaG6rwlQp8H7bSf5AN5o130_provenance.
- NP371019.RAxIwKSUM_xhV1tXZLfkmwcBzSaG6rwlQp8H7bSf5AN5o130_assertion description "[We confirmed the finding of an increased frequency of the C4B null allele in autism and found that the related disorders also had an increased frequency of this null allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP371019.RAxIwKSUM_xhV1tXZLfkmwcBzSaG6rwlQp8H7bSf5AN5o130_provenance.
- NP371019.RAxIwKSUM_xhV1tXZLfkmwcBzSaG6rwlQp8H7bSf5AN5o130_assertion evidence source_evidence_literature NP371019.RAxIwKSUM_xhV1tXZLfkmwcBzSaG6rwlQp8H7bSf5AN5o130_provenance.
- NP371019.RAxIwKSUM_xhV1tXZLfkmwcBzSaG6rwlQp8H7bSf5AN5o130_assertion SIO_000772 8871944 NP371019.RAxIwKSUM_xhV1tXZLfkmwcBzSaG6rwlQp8H7bSf5AN5o130_provenance.
- NP371019.RAxIwKSUM_xhV1tXZLfkmwcBzSaG6rwlQp8H7bSf5AN5o130_assertion wasDerivedFrom befree-20140225 NP371019.RAxIwKSUM_xhV1tXZLfkmwcBzSaG6rwlQp8H7bSf5AN5o130_provenance.
- NP371019.RAxIwKSUM_xhV1tXZLfkmwcBzSaG6rwlQp8H7bSf5AN5o130_assertion wasGeneratedBy ECO_0000203 NP371019.RAxIwKSUM_xhV1tXZLfkmwcBzSaG6rwlQp8H7bSf5AN5o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP371019.RAxIwKSUM_xhV1tXZLfkmwcBzSaG6rwlQp8H7bSf5AN5o130_provenance.