Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP246887.RAUDSPvj6_bjrnUetn1Zd-_1q-m7ST4tlKtmxhRn3S580130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP246887.RAUDSPvj6_bjrnUetn1Zd-_1q-m7ST4tlKtmxhRn3S580130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP246887.RAUDSPvj6_bjrnUetn1Zd-_1q-m7ST4tlKtmxhRn3S580130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP246887.RAUDSPvj6_bjrnUetn1Zd-_1q-m7ST4tlKtmxhRn3S580130_provenance.
- NP246887.RAUDSPvj6_bjrnUetn1Zd-_1q-m7ST4tlKtmxhRn3S580130_assertion description "[The risk of spontaneous or risk-period related venous thromboembolism in family members of symptomatic carriers of antithrombin (AT), protein C (PC) or protein S (PS) defects, as well as of the Factor V Leiden mutation is still undefined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP246887.RAUDSPvj6_bjrnUetn1Zd-_1q-m7ST4tlKtmxhRn3S580130_provenance.
- NP246887.RAUDSPvj6_bjrnUetn1Zd-_1q-m7ST4tlKtmxhRn3S580130_assertion evidence source_evidence_literature NP246887.RAUDSPvj6_bjrnUetn1Zd-_1q-m7ST4tlKtmxhRn3S580130_provenance.
- NP246887.RAUDSPvj6_bjrnUetn1Zd-_1q-m7ST4tlKtmxhRn3S580130_assertion SIO_000772 10063991 NP246887.RAUDSPvj6_bjrnUetn1Zd-_1q-m7ST4tlKtmxhRn3S580130_provenance.
- NP246887.RAUDSPvj6_bjrnUetn1Zd-_1q-m7ST4tlKtmxhRn3S580130_assertion wasDerivedFrom befree-2016 NP246887.RAUDSPvj6_bjrnUetn1Zd-_1q-m7ST4tlKtmxhRn3S580130_provenance.
- NP246887.RAUDSPvj6_bjrnUetn1Zd-_1q-m7ST4tlKtmxhRn3S580130_assertion wasGeneratedBy ECO_0000203 NP246887.RAUDSPvj6_bjrnUetn1Zd-_1q-m7ST4tlKtmxhRn3S580130_provenance.
- befree-2016 importedOn "2016-02-19" NP246887.RAUDSPvj6_bjrnUetn1Zd-_1q-m7ST4tlKtmxhRn3S580130_provenance.