Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_assertion> ?p ?o ?g. }
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- NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_assertion type Assertion NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_head.
- NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_assertion description "[Dentinogenesis imperfecta type II and dentin dysplasia type II are diseases resulting in abnormal dentin formation, which have been mapped to overlapping regions of human chromosome 4q defined by markers D4S2691 and D4S2692 (6.6 cM) and D4S3291 and SPP1 (14.1 cM), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_provenance.
- NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_assertion evidence source_evidence_literature NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_provenance.
- NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_assertion SIO_000772 9541230 NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_provenance.
- NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_assertion wasDerivedFrom befree-20140225 NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_provenance.
- NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_assertion wasGeneratedBy ECO_0000203 NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_provenance.