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- source_evidence_literature type ECO_0000212 NP589765.RAoZ5pszaFp-bSfKz_6r3G36SmJcrSJdMty977jdSdKvU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP589765.RAoZ5pszaFp-bSfKz_6r3G36SmJcrSJdMty977jdSdKvU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP589765.RAoZ5pszaFp-bSfKz_6r3G36SmJcrSJdMty977jdSdKvU130_provenance.
- NP589765.RAoZ5pszaFp-bSfKz_6r3G36SmJcrSJdMty977jdSdKvU130_assertion description "[Here we report on a second BFNC family in which linkage to the EBN1 locus on chromosome 20q was excluded, confirming the genetic heterogeneity of this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP589765.RAoZ5pszaFp-bSfKz_6r3G36SmJcrSJdMty977jdSdKvU130_provenance.
- NP589765.RAoZ5pszaFp-bSfKz_6r3G36SmJcrSJdMty977jdSdKvU130_assertion evidence source_evidence_literature NP589765.RAoZ5pszaFp-bSfKz_6r3G36SmJcrSJdMty977jdSdKvU130_provenance.
- NP589765.RAoZ5pszaFp-bSfKz_6r3G36SmJcrSJdMty977jdSdKvU130_assertion SIO_000772 7705837 NP589765.RAoZ5pszaFp-bSfKz_6r3G36SmJcrSJdMty977jdSdKvU130_provenance.
- NP589765.RAoZ5pszaFp-bSfKz_6r3G36SmJcrSJdMty977jdSdKvU130_assertion wasDerivedFrom befree-20140225 NP589765.RAoZ5pszaFp-bSfKz_6r3G36SmJcrSJdMty977jdSdKvU130_provenance.
- NP589765.RAoZ5pszaFp-bSfKz_6r3G36SmJcrSJdMty977jdSdKvU130_assertion wasGeneratedBy ECO_0000203 NP589765.RAoZ5pszaFp-bSfKz_6r3G36SmJcrSJdMty977jdSdKvU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP589765.RAoZ5pszaFp-bSfKz_6r3G36SmJcrSJdMty977jdSdKvU130_provenance.