Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP641814.RAUF0_096n4BZpQPoDACf4WAdawc50PwhCSeY8pTIXCjQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP641814.RAUF0_096n4BZpQPoDACf4WAdawc50PwhCSeY8pTIXCjQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP641814.RAUF0_096n4BZpQPoDACf4WAdawc50PwhCSeY8pTIXCjQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP641814.RAUF0_096n4BZpQPoDACf4WAdawc50PwhCSeY8pTIXCjQ130_provenance.
- NP641814.RAUF0_096n4BZpQPoDACf4WAdawc50PwhCSeY8pTIXCjQ130_assertion wasGeneratedBy ECO_0000203 NP641814.RAUF0_096n4BZpQPoDACf4WAdawc50PwhCSeY8pTIXCjQ130_provenance.
- NP641814.RAUF0_096n4BZpQPoDACf4WAdawc50PwhCSeY8pTIXCjQ130_assertion wasDerivedFrom befree-20140225 NP641814.RAUF0_096n4BZpQPoDACf4WAdawc50PwhCSeY8pTIXCjQ130_provenance.
- NP641814.RAUF0_096n4BZpQPoDACf4WAdawc50PwhCSeY8pTIXCjQ130_assertion SIO_000772 22310223 NP641814.RAUF0_096n4BZpQPoDACf4WAdawc50PwhCSeY8pTIXCjQ130_provenance.
- NP641814.RAUF0_096n4BZpQPoDACf4WAdawc50PwhCSeY8pTIXCjQ130_assertion evidence source_evidence_literature NP641814.RAUF0_096n4BZpQPoDACf4WAdawc50PwhCSeY8pTIXCjQ130_provenance.
- NP641814.RAUF0_096n4BZpQPoDACf4WAdawc50PwhCSeY8pTIXCjQ130_assertion description "[Clinical molecular diagnostic centers routinely screen SHH, ZIC2, SIX3 and TGIF for mutations that can help to explain holoprosencephaly and related brain malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP641814.RAUF0_096n4BZpQPoDACf4WAdawc50PwhCSeY8pTIXCjQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP641814.RAUF0_096n4BZpQPoDACf4WAdawc50PwhCSeY8pTIXCjQ130_provenance.