Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP869311.RAPLlxBe--mZ9DisouDtpw-ccYq-U6SXfRdquEn77HTmE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP869311.RAPLlxBe--mZ9DisouDtpw-ccYq-U6SXfRdquEn77HTmE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869311.RAPLlxBe--mZ9DisouDtpw-ccYq-U6SXfRdquEn77HTmE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869311.RAPLlxBe--mZ9DisouDtpw-ccYq-U6SXfRdquEn77HTmE130_provenance.
- NP869311.RAPLlxBe--mZ9DisouDtpw-ccYq-U6SXfRdquEn77HTmE130_assertion wasGeneratedBy ECO_0000203 NP869311.RAPLlxBe--mZ9DisouDtpw-ccYq-U6SXfRdquEn77HTmE130_provenance.
- NP869311.RAPLlxBe--mZ9DisouDtpw-ccYq-U6SXfRdquEn77HTmE130_assertion wasDerivedFrom befree-20140225 NP869311.RAPLlxBe--mZ9DisouDtpw-ccYq-U6SXfRdquEn77HTmE130_provenance.
- NP869311.RAPLlxBe--mZ9DisouDtpw-ccYq-U6SXfRdquEn77HTmE130_assertion SIO_000772 9615224 NP869311.RAPLlxBe--mZ9DisouDtpw-ccYq-U6SXfRdquEn77HTmE130_provenance.
- NP869311.RAPLlxBe--mZ9DisouDtpw-ccYq-U6SXfRdquEn77HTmE130_assertion evidence source_evidence_literature NP869311.RAPLlxBe--mZ9DisouDtpw-ccYq-U6SXfRdquEn77HTmE130_provenance.
- NP869311.RAPLlxBe--mZ9DisouDtpw-ccYq-U6SXfRdquEn77HTmE130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869311.RAPLlxBe--mZ9DisouDtpw-ccYq-U6SXfRdquEn77HTmE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP869311.RAPLlxBe--mZ9DisouDtpw-ccYq-U6SXfRdquEn77HTmE130_provenance.