Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP233261.RA6DikB1EKazlqLE_IpR7TxKC_5uZD10WQqsH-VNj2Xro130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP233261.RA6DikB1EKazlqLE_IpR7TxKC_5uZD10WQqsH-VNj2Xro130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP233261.RA6DikB1EKazlqLE_IpR7TxKC_5uZD10WQqsH-VNj2Xro130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP233261.RA6DikB1EKazlqLE_IpR7TxKC_5uZD10WQqsH-VNj2Xro130_provenance.
- NP233261.RA6DikB1EKazlqLE_IpR7TxKC_5uZD10WQqsH-VNj2Xro130_assertion description "[About 30% of the mutations causing nonsyndromic X-linked mental retardation (MRX) are thought to be located in Xp11 and in the pericentromeric region, with a particular clustering of gene defects in a 7.4 Mb interval flanked by the genes ELK1 and ALAS2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP233261.RA6DikB1EKazlqLE_IpR7TxKC_5uZD10WQqsH-VNj2Xro130_provenance.
- NP233261.RA6DikB1EKazlqLE_IpR7TxKC_5uZD10WQqsH-VNj2Xro130_assertion evidence source_evidence_literature NP233261.RA6DikB1EKazlqLE_IpR7TxKC_5uZD10WQqsH-VNj2Xro130_provenance.
- NP233261.RA6DikB1EKazlqLE_IpR7TxKC_5uZD10WQqsH-VNj2Xro130_assertion SIO_000772 16969374 NP233261.RA6DikB1EKazlqLE_IpR7TxKC_5uZD10WQqsH-VNj2Xro130_provenance.
- NP233261.RA6DikB1EKazlqLE_IpR7TxKC_5uZD10WQqsH-VNj2Xro130_assertion wasDerivedFrom befree-20150227 NP233261.RA6DikB1EKazlqLE_IpR7TxKC_5uZD10WQqsH-VNj2Xro130_provenance.
- NP233261.RA6DikB1EKazlqLE_IpR7TxKC_5uZD10WQqsH-VNj2Xro130_assertion wasGeneratedBy ECO_0000203 NP233261.RA6DikB1EKazlqLE_IpR7TxKC_5uZD10WQqsH-VNj2Xro130_provenance.
- befree-20150227 importedOn "2015-02-27" NP233261.RA6DikB1EKazlqLE_IpR7TxKC_5uZD10WQqsH-VNj2Xro130_provenance.