Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP547971.RAX2PN9LFUpwU9SgDJK9lHEX-twXpHdvpdVN3K70fk2RA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP547971.RAX2PN9LFUpwU9SgDJK9lHEX-twXpHdvpdVN3K70fk2RA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP547971.RAX2PN9LFUpwU9SgDJK9lHEX-twXpHdvpdVN3K70fk2RA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP547971.RAX2PN9LFUpwU9SgDJK9lHEX-twXpHdvpdVN3K70fk2RA130_provenance.
- NP547971.RAX2PN9LFUpwU9SgDJK9lHEX-twXpHdvpdVN3K70fk2RA130_assertion description "[Further study of this family may help define those genes functioning in the MBP region that contribute to the phenotype of 18q- syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547971.RAX2PN9LFUpwU9SgDJK9lHEX-twXpHdvpdVN3K70fk2RA130_provenance.
- NP547971.RAX2PN9LFUpwU9SgDJK9lHEX-twXpHdvpdVN3K70fk2RA130_assertion evidence source_evidence_literature NP547971.RAX2PN9LFUpwU9SgDJK9lHEX-twXpHdvpdVN3K70fk2RA130_provenance.
- NP547971.RAX2PN9LFUpwU9SgDJK9lHEX-twXpHdvpdVN3K70fk2RA130_assertion SIO_000772 9556294 NP547971.RAX2PN9LFUpwU9SgDJK9lHEX-twXpHdvpdVN3K70fk2RA130_provenance.
- NP547971.RAX2PN9LFUpwU9SgDJK9lHEX-twXpHdvpdVN3K70fk2RA130_assertion wasDerivedFrom befree-20150227 NP547971.RAX2PN9LFUpwU9SgDJK9lHEX-twXpHdvpdVN3K70fk2RA130_provenance.
- NP547971.RAX2PN9LFUpwU9SgDJK9lHEX-twXpHdvpdVN3K70fk2RA130_assertion wasGeneratedBy ECO_0000203 NP547971.RAX2PN9LFUpwU9SgDJK9lHEX-twXpHdvpdVN3K70fk2RA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP547971.RAX2PN9LFUpwU9SgDJK9lHEX-twXpHdvpdVN3K70fk2RA130_provenance.