Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP641814.RAUF0_096n4BZpQPoDACf4WAdawc50PwhCSeY8pTIXCjQ130_assertion> ?p ?o ?g. }
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- NP641814.RAUF0_096n4BZpQPoDACf4WAdawc50PwhCSeY8pTIXCjQ130_assertion type Assertion NP641814.RAUF0_096n4BZpQPoDACf4WAdawc50PwhCSeY8pTIXCjQ130_head.
- 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.