Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1327681.RAkpPfsQqnDWZXKwr3yrE1hZrvjKhZ9wG9rJS7u2e2cB0130_assertion> ?p ?o ?g. }
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- NP1327681.RAkpPfsQqnDWZXKwr3yrE1hZrvjKhZ9wG9rJS7u2e2cB0130_assertion type Assertion NP1327681.RAkpPfsQqnDWZXKwr3yrE1hZrvjKhZ9wG9rJS7u2e2cB0130_head.
- NP1327681.RAkpPfsQqnDWZXKwr3yrE1hZrvjKhZ9wG9rJS7u2e2cB0130_assertion description "[No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327681.RAkpPfsQqnDWZXKwr3yrE1hZrvjKhZ9wG9rJS7u2e2cB0130_provenance.
- NP1327681.RAkpPfsQqnDWZXKwr3yrE1hZrvjKhZ9wG9rJS7u2e2cB0130_assertion evidence source_evidence_literature NP1327681.RAkpPfsQqnDWZXKwr3yrE1hZrvjKhZ9wG9rJS7u2e2cB0130_provenance.
- NP1327681.RAkpPfsQqnDWZXKwr3yrE1hZrvjKhZ9wG9rJS7u2e2cB0130_assertion SIO_000772 7942992 NP1327681.RAkpPfsQqnDWZXKwr3yrE1hZrvjKhZ9wG9rJS7u2e2cB0130_provenance.
- NP1327681.RAkpPfsQqnDWZXKwr3yrE1hZrvjKhZ9wG9rJS7u2e2cB0130_assertion wasDerivedFrom befree-2016 NP1327681.RAkpPfsQqnDWZXKwr3yrE1hZrvjKhZ9wG9rJS7u2e2cB0130_provenance.
- NP1327681.RAkpPfsQqnDWZXKwr3yrE1hZrvjKhZ9wG9rJS7u2e2cB0130_assertion wasGeneratedBy ECO_0000203 NP1327681.RAkpPfsQqnDWZXKwr3yrE1hZrvjKhZ9wG9rJS7u2e2cB0130_provenance.