Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP958978.RAodPWSpI79Tyc80SJzxS53U67t7m29OIWvD1pj2y4W1U130_assertion> ?p ?o ?g. }
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- NP958978.RAodPWSpI79Tyc80SJzxS53U67t7m29OIWvD1pj2y4W1U130_assertion type Assertion NP958978.RAodPWSpI79Tyc80SJzxS53U67t7m29OIWvD1pj2y4W1U130_head.
- NP958978.RAodPWSpI79Tyc80SJzxS53U67t7m29OIWvD1pj2y4W1U130_assertion wasGeneratedBy ECO_0000203 NP958978.RAodPWSpI79Tyc80SJzxS53U67t7m29OIWvD1pj2y4W1U130_provenance.
- NP958978.RAodPWSpI79Tyc80SJzxS53U67t7m29OIWvD1pj2y4W1U130_assertion wasDerivedFrom befree-2016 NP958978.RAodPWSpI79Tyc80SJzxS53U67t7m29OIWvD1pj2y4W1U130_provenance.
- NP958978.RAodPWSpI79Tyc80SJzxS53U67t7m29OIWvD1pj2y4W1U130_assertion SIO_000772 22310223 NP958978.RAodPWSpI79Tyc80SJzxS53U67t7m29OIWvD1pj2y4W1U130_provenance.
- NP958978.RAodPWSpI79Tyc80SJzxS53U67t7m29OIWvD1pj2y4W1U130_assertion evidence source_evidence_literature NP958978.RAodPWSpI79Tyc80SJzxS53U67t7m29OIWvD1pj2y4W1U130_provenance.
- NP958978.RAodPWSpI79Tyc80SJzxS53U67t7m29OIWvD1pj2y4W1U130_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." NP958978.RAodPWSpI79Tyc80SJzxS53U67t7m29OIWvD1pj2y4W1U130_provenance.