Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP665637.RAkmub0fgMljOtQW5HBA7CGPq4DuDm2y1VJPcE-rI1dQw130_assertion> ?p ?o ?g. }
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- NP665637.RAkmub0fgMljOtQW5HBA7CGPq4DuDm2y1VJPcE-rI1dQw130_assertion type Assertion NP665637.RAkmub0fgMljOtQW5HBA7CGPq4DuDm2y1VJPcE-rI1dQw130_head.
- NP665637.RAkmub0fgMljOtQW5HBA7CGPq4DuDm2y1VJPcE-rI1dQw130_assertion description "[All patients with POMT1 and POMT2 mutations had evidence of either structural or functional central nervous system involvement including four patients with mental retardation and a LGMD phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665637.RAkmub0fgMljOtQW5HBA7CGPq4DuDm2y1VJPcE-rI1dQw130_provenance.
- NP665637.RAkmub0fgMljOtQW5HBA7CGPq4DuDm2y1VJPcE-rI1dQw130_assertion evidence source_evidence_literature NP665637.RAkmub0fgMljOtQW5HBA7CGPq4DuDm2y1VJPcE-rI1dQw130_provenance.
- NP665637.RAkmub0fgMljOtQW5HBA7CGPq4DuDm2y1VJPcE-rI1dQw130_assertion SIO_000772 17878207 NP665637.RAkmub0fgMljOtQW5HBA7CGPq4DuDm2y1VJPcE-rI1dQw130_provenance.
- NP665637.RAkmub0fgMljOtQW5HBA7CGPq4DuDm2y1VJPcE-rI1dQw130_assertion wasDerivedFrom befree-20140225 NP665637.RAkmub0fgMljOtQW5HBA7CGPq4DuDm2y1VJPcE-rI1dQw130_provenance.
- NP665637.RAkmub0fgMljOtQW5HBA7CGPq4DuDm2y1VJPcE-rI1dQw130_assertion wasGeneratedBy ECO_0000203 NP665637.RAkmub0fgMljOtQW5HBA7CGPq4DuDm2y1VJPcE-rI1dQw130_provenance.