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- NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_assertion type Assertion NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_head.
- NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_assertion description "[Mutation analysis of the ALX4 gene in three unrelated FPP families without the MSX2 mutation identified mutations in two families, indicating that mutations in ALX4 could be responsible for these skull defects and suggesting further genetic heterogeneity of FPP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_provenance.
- NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_assertion evidence source_evidence_literature NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_provenance.
- NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_assertion SIO_000772 11106354 NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_provenance.
- NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_assertion wasDerivedFrom befree-20150227 NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_provenance.
- NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_assertion wasGeneratedBy ECO_0000203 NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_provenance.