Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP665637.RAkmub0fgMljOtQW5HBA7CGPq4DuDm2y1VJPcE-rI1dQw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP665637.RAkmub0fgMljOtQW5HBA7CGPq4DuDm2y1VJPcE-rI1dQw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP665637.RAkmub0fgMljOtQW5HBA7CGPq4DuDm2y1VJPcE-rI1dQw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP665637.RAkmub0fgMljOtQW5HBA7CGPq4DuDm2y1VJPcE-rI1dQw130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP665637.RAkmub0fgMljOtQW5HBA7CGPq4DuDm2y1VJPcE-rI1dQw130_provenance.