Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1343149.RAwpTrJg5UY-_qtbMstJDpyyHBo9sS6QiSd2S1JxZID7s130_assertion> ?p ?o ?g. }
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- NP1343149.RAwpTrJg5UY-_qtbMstJDpyyHBo9sS6QiSd2S1JxZID7s130_assertion type Assertion NP1343149.RAwpTrJg5UY-_qtbMstJDpyyHBo9sS6QiSd2S1JxZID7s130_head.
- NP1343149.RAwpTrJg5UY-_qtbMstJDpyyHBo9sS6QiSd2S1JxZID7s130_assertion description "[Our results suggest that mutations in FMR-1 are directly responsible for fragile X syndrome, irrespective of possible secondary effects caused by FRAXA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1343149.RAwpTrJg5UY-_qtbMstJDpyyHBo9sS6QiSd2S1JxZID7s130_provenance.
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- NP1343149.RAwpTrJg5UY-_qtbMstJDpyyHBo9sS6QiSd2S1JxZID7s130_assertion SIO_000772 8490650 NP1343149.RAwpTrJg5UY-_qtbMstJDpyyHBo9sS6QiSd2S1JxZID7s130_provenance.
- NP1343149.RAwpTrJg5UY-_qtbMstJDpyyHBo9sS6QiSd2S1JxZID7s130_assertion wasDerivedFrom befree-2016 NP1343149.RAwpTrJg5UY-_qtbMstJDpyyHBo9sS6QiSd2S1JxZID7s130_provenance.
- NP1343149.RAwpTrJg5UY-_qtbMstJDpyyHBo9sS6QiSd2S1JxZID7s130_assertion wasGeneratedBy ECO_0000203 NP1343149.RAwpTrJg5UY-_qtbMstJDpyyHBo9sS6QiSd2S1JxZID7s130_provenance.