Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP802654.RAT-w2X2bd61HlHQwSmVo-mFwHJ_XJzLG3egn79TVaHRg130_assertion> ?p ?o ?g. }
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- NP802654.RAT-w2X2bd61HlHQwSmVo-mFwHJ_XJzLG3egn79TVaHRg130_assertion type Assertion NP802654.RAT-w2X2bd61HlHQwSmVo-mFwHJ_XJzLG3egn79TVaHRg130_head.
- NP802654.RAT-w2X2bd61HlHQwSmVo-mFwHJ_XJzLG3egn79TVaHRg130_assertion description "[Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802654.RAT-w2X2bd61HlHQwSmVo-mFwHJ_XJzLG3egn79TVaHRg130_provenance.
- NP802654.RAT-w2X2bd61HlHQwSmVo-mFwHJ_XJzLG3egn79TVaHRg130_assertion evidence source_evidence_literature NP802654.RAT-w2X2bd61HlHQwSmVo-mFwHJ_XJzLG3egn79TVaHRg130_provenance.
- NP802654.RAT-w2X2bd61HlHQwSmVo-mFwHJ_XJzLG3egn79TVaHRg130_assertion SIO_000772 17655765 NP802654.RAT-w2X2bd61HlHQwSmVo-mFwHJ_XJzLG3egn79TVaHRg130_provenance.
- NP802654.RAT-w2X2bd61HlHQwSmVo-mFwHJ_XJzLG3egn79TVaHRg130_assertion wasDerivedFrom befree-20150227 NP802654.RAT-w2X2bd61HlHQwSmVo-mFwHJ_XJzLG3egn79TVaHRg130_provenance.
- NP802654.RAT-w2X2bd61HlHQwSmVo-mFwHJ_XJzLG3egn79TVaHRg130_assertion wasGeneratedBy ECO_0000203 NP802654.RAT-w2X2bd61HlHQwSmVo-mFwHJ_XJzLG3egn79TVaHRg130_provenance.