Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP409235.RAofKLeEp7m8ORElf7gTEVL2-wKvQpCL3JV4af80TLW-w130_assertion> ?p ?o ?g. }
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- NP409235.RAofKLeEp7m8ORElf7gTEVL2-wKvQpCL3JV4af80TLW-w130_assertion type Assertion NP409235.RAofKLeEp7m8ORElf7gTEVL2-wKvQpCL3JV4af80TLW-w130_head.
- NP409235.RAofKLeEp7m8ORElf7gTEVL2-wKvQpCL3JV4af80TLW-w130_assertion description "[Our observation demonstrates that FMR2 gene deletions may contribute to the FRAXE phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409235.RAofKLeEp7m8ORElf7gTEVL2-wKvQpCL3JV4af80TLW-w130_provenance.
- NP409235.RAofKLeEp7m8ORElf7gTEVL2-wKvQpCL3JV4af80TLW-w130_assertion evidence source_evidence_literature NP409235.RAofKLeEp7m8ORElf7gTEVL2-wKvQpCL3JV4af80TLW-w130_provenance.
- NP409235.RAofKLeEp7m8ORElf7gTEVL2-wKvQpCL3JV4af80TLW-w130_assertion SIO_000772 21739600 NP409235.RAofKLeEp7m8ORElf7gTEVL2-wKvQpCL3JV4af80TLW-w130_provenance.
- NP409235.RAofKLeEp7m8ORElf7gTEVL2-wKvQpCL3JV4af80TLW-w130_assertion wasDerivedFrom befree-20150227 NP409235.RAofKLeEp7m8ORElf7gTEVL2-wKvQpCL3JV4af80TLW-w130_provenance.
- NP409235.RAofKLeEp7m8ORElf7gTEVL2-wKvQpCL3JV4af80TLW-w130_assertion wasGeneratedBy ECO_0000203 NP409235.RAofKLeEp7m8ORElf7gTEVL2-wKvQpCL3JV4af80TLW-w130_provenance.