Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1181466.RAd6mDXyWoQzikHKU9iTNMzFatZ_s3TBSjm41QEKPl-Pw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1181466.RAd6mDXyWoQzikHKU9iTNMzFatZ_s3TBSjm41QEKPl-Pw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1181466.RAd6mDXyWoQzikHKU9iTNMzFatZ_s3TBSjm41QEKPl-Pw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1181466.RAd6mDXyWoQzikHKU9iTNMzFatZ_s3TBSjm41QEKPl-Pw130_provenance.
- NP1181466.RAd6mDXyWoQzikHKU9iTNMzFatZ_s3TBSjm41QEKPl-Pw130_assertion description "[Our findings suggest a role for OTX2 dosage sensitivity in human craniofacial development and raise the possibility of a shared etiology between a subtype of hemifacial microsomia and medulloblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1181466.RAd6mDXyWoQzikHKU9iTNMzFatZ_s3TBSjm41QEKPl-Pw130_provenance.
- NP1181466.RAd6mDXyWoQzikHKU9iTNMzFatZ_s3TBSjm41QEKPl-Pw130_assertion evidence source_evidence_literature NP1181466.RAd6mDXyWoQzikHKU9iTNMzFatZ_s3TBSjm41QEKPl-Pw130_provenance.
- NP1181466.RAd6mDXyWoQzikHKU9iTNMzFatZ_s3TBSjm41QEKPl-Pw130_assertion SIO_000772 24816892 NP1181466.RAd6mDXyWoQzikHKU9iTNMzFatZ_s3TBSjm41QEKPl-Pw130_provenance.
- NP1181466.RAd6mDXyWoQzikHKU9iTNMzFatZ_s3TBSjm41QEKPl-Pw130_assertion wasDerivedFrom befree-2016 NP1181466.RAd6mDXyWoQzikHKU9iTNMzFatZ_s3TBSjm41QEKPl-Pw130_provenance.
- NP1181466.RAd6mDXyWoQzikHKU9iTNMzFatZ_s3TBSjm41QEKPl-Pw130_assertion wasGeneratedBy ECO_0000203 NP1181466.RAd6mDXyWoQzikHKU9iTNMzFatZ_s3TBSjm41QEKPl-Pw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1181466.RAd6mDXyWoQzikHKU9iTNMzFatZ_s3TBSjm41QEKPl-Pw130_provenance.