Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_assertion> ?p ?o ?g. }
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- NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_assertion type Assertion NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_head.
- NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_assertion description "[New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_provenance.
- NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_assertion evidence source_evidence_curated NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_provenance.
- NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_assertion SIO_000772 11030761 NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_provenance.
- NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_assertion wasDerivedFrom uniprot-20130724 NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_provenance.
- NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_assertion wasGeneratedBy ECO_0000218 NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_provenance.